Variant report

Variant rs184175169
Chromosome Location chr2:234654900-234654901
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr2:234652800-234658200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr2:234652800-234659200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr2:234653200-234655600 Enhancers Fetal Intestine Small intestine
9 chr2:234654200-234655000 Enhancers A549 lung
10 chr2:234654200-234655400 Enhancers Duodenum Mucosa Duodenum
11 chr2:234654200-234655400 Enhancers Fetal Intestine Large intestine
12 chr2:234654400-234656000 Flanking Active TSS Liver Liver
13 chr2:234654600-234655800 Bivalent Enhancer HepG2 liver

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