Variant report

Variant rs9613976
Chromosome Location chr22:29985012-29985013
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:29977600-29998800 Weak transcription Right Atrium heart
2 chr22:29977800-29994200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr22:29979000-29990000 Weak transcription K562 blood
4 chr22:29983600-29985200 Enhancers NHDF-Ad bronchial
5 chr22:29983600-29985400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr22:29983800-29985200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr22:29983800-29985200 Enhancers NHEK skin
8 chr22:29984000-29985200 Flanking Active TSS HepG2 liver
9 chr22:29984400-29985200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr22:29984400-29985400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr22:29984400-29985400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr22:29984600-29986200 Weak transcription Muscle Satellite Cultured Cells --
13 chr22:29984600-29986600 Weak transcription Hela-S3 cervix
14 chr22:29984600-29990000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr22:29984800-29986200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
16 chr22:29985000-29989800 Weak transcription A549 lung

Quick Search:


  
Input of quick search could be:

what's new

Quick links