UCSC Genome Browser on Human (GRCh38/hg38)
move zoom in zoom out
chr6:152,833,977-152,869,864 35,888 bp.
move start
  Click on a feature for details. Click+shift+drag to zoom in. Click side bars for track options. Drag side bars or labels up or down to reorder tracks. Drag tracks left or right to new position. Press "?" for keyboard shortcuts.   move end
  
Use drop-down controls below and press refresh to alter tracks displayed.
Tracks with lots of items will automatically be displayed in more compact modes.
-   Custom Tracks
170613_L1neg
170613_L1pos
170613_L2pos
170613_L3pos
170613_L4pos
170613_L5neg
170613_L5pos
170613_L6pos
170620_L1pos
170620_L2pos
170620_L3pos
170620_L4pos
170620_L5neg
170620_L5pos
170620_L6pos
170711-L1neg
170711-L1pos
170711-L2pos
170711-L3pos
170711-L4pos
170711-L5neg
170711-L5pos
170711-L6pos
CamK2a_liftOver
Cux2_liftOver
Exc_pks
Exc_pks_010218
Exc_pks_600bp
Gad2_liftOver
GenomicCtrl_liftOver
HGT_CRMs
Inh_pks
Inh_pks_010218
Inh_pks_600bp
L1neg_pks
L1neg_reads
L1pos_pks
L1pos_reads
L2pos_pks
L2pos_reads
L3pos_pks
L3pos_reads
L4pos_pks
L4pos_reads
L5neg_pks
L5neg_reads
L5pos_pks
L5pos_reads
L6pos_pks
L6pos_reads
Lake2017_Exc
Lake2017_Inh
mESC_liftOver
Ntsr1_liftOver
Pvalb_liftOver
Rbp4_liftOver
Scnn1a-Tg3_liftOver
Sst_liftOver
Vip_liftOver
-   Mapping and Sequencing
Base Position
p13 Fix Patches
p13 Alt Haplotypes
Assembly
Centromeres
Chromosome Band
Clone Ends
Exome Probesets
FISH Clones
Gap
GC Percent
GRC Contigs
GRC Incident
Hg19 Diff
INSDC
LiftOver & ReMap
LRG Regions
Mappability
RefSeq Acc
Restr Enzymes
Scaffolds
Short Match
STS Markers
-   Genes and Gene Predictions
updated GENCODE V41
NCBI RefSeq
new All GENCODE
CCDS
CRISPR Targets
IKMC Genes Mapped
LRG Transcripts
MANE v1.0
MGC Genes
Non-coding RNA
Old UCSC Genes
ORFeome Clones
Other RefSeq
Pfam in GENCODE
Prediction Archive
RetroGenes V9
TransMap V5
UCSC Alt Events
UniProt
-   Phenotype and Literature
OMIM Alleles
CADD
Cancer Gene Expr
ClinGen
ClinGen CNVs
ClinVar Variants
Constraint scores
Coriell CNVs
COSMIC Regions
new DECIPHER CNVs
new DECIPHER SNVs
Development Delay
new GenCC
Gene Interactions
GeneReviews
GWAS Catalog
HGMD Variants
LOVD Variants
OMIM Cyto Loci
OMIM Genes
Orphanet
REVEL Scores
SNPedia
TCGA Pan-Cancer
UniProt Variants
Variants in Papers
-   COVID-19
COVID GWAS v4
COVID GWAS v3
Rare Harmful Vars
-   Single Cell RNA-seq
Blood (PBMC) Hao
Colon Wang
Cortex Velmeshev
Fetal Gene Atlas
Heart Cell Atlas
Ileum Wang
Kidney Stewart
Liver MacParland
Lung Travaglini
new Merged Cells
Muscle De Micheli
Pancreas Baron
Placenta Vento-Tormo
Rectum Wang
Skin Sole-Boldo
new Tabula Sapiens
-   mRNA and EST
Human ESTs
Human mRNAs
Other ESTs
Other mRNAs
SIB Alt-Splicing
Spliced ESTs
-   Expression
GTEx Gene V8
GTEx RNA-Seq Coverage
Affy Archive
EPDnew Promoters
GNF Atlas 2
GTEx Gene
GTEx Transcript
GWIPS-viz Riboseq
miRNA Tissue Atlas
-   Regulation
ENCODE cCREs
ENCODE Regulation
CpG Islands
GeneHancer
new GTEx cis-eQTLs
Hi-C and Micro-C
JASPAR Transcription Factors
ORegAnno
RefSeq Func Elems
new ReMap ChIP-seq
-   Comparative Genomics
Conservation
Cactus 241-way
Cons 30 Primates
Primate Chain/Net
Placental Chain/Net
Vertebrate Chain/Net
CHM13 alignments
Human Chain/Net
-   Variation
dbSNP 153
1000G Archive
new Array Probsets
dbSNP Archive
dbVar Common Struct Var
DGV Struct Var
Genome In a Bottle
updated gnomAD Variants
Platinum Genomes
-   Repeats
RepeatMasker
Interrupted Rpts
Microsatellite
RepeatMasker Viz.
Segmental Dups
Self Chain
Simple Repeats
WM + SDust
Invisible link