Variant report

Variant rs568702968
Chromosome Location chr2:234652449-234652450
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:234620400-234659200 Weak transcription Colonic Mucosa Colon
2 chr2:234626600-234668400 Weak transcription NHEK skin
3 chr2:234646400-234666600 Weak transcription Stomach Mucosa stomach
4 chr2:234647800-234655000 Weak transcription Gastric stomach
5 chr2:234649800-234658800 Weak transcription Rectal Mucosa Donor 29 rectum
6 chr2:234650400-234652600 Genic enhancers Liver Liver
7 chr2:234651000-234652800 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr2:234652200-234652600 ZNF genes & repeats iPS DF 6.9 Cell Line embryonic stem cell
9 chr2:234652200-234652600 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
10 chr2:234652200-234652600 ZNF genes & repeats Esophagus oesophagus
11 chr2:234652200-234652800 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr2:234652400-234652600 Flanking Active TSS H1 Derived Mesenchymal Stem Cells ES cell derived

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