Variant report

Variant rs28899468
Chromosome Location chr2:234653292-234653293
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 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 chr2:234652600-234654400 Enhancers Liver Liver
7 chr2:234652600-234654600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr2:234652800-234658200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr2:234652800-234659200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr2:234653200-234654400 Enhancers HepG2 liver
11 chr2:234653200-234655600 Enhancers Fetal Intestine Small intestine

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