Variant report

Variant rs145191619
Chromosome Location chr16:82061189-82061190
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:82058000-82065600 Weak transcription Gastric stomach
2 chr16:82058600-82062400 Enhancers Duodenum Mucosa Duodenum
3 chr16:82059400-82062200 Enhancers Fetal Intestine Large intestine
4 chr16:82060000-82062000 Enhancers Fetal Intestine Small intestine
5 chr16:82060600-82061800 Weak transcription Small Intestine intestine
6 chr16:82060600-82062000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr16:82060600-82062200 Enhancers NHEK skin
8 chr16:82060800-82061400 Enhancers HMEC breast
9 chr16:82060800-82062000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr16:82060800-82062200 Enhancers Liver Liver
11 chr16:82061000-82062000 Enhancers Stomach Mucosa stomach
12 chr16:82061000-82066600 Weak transcription Pancreas Pancrea
13 chr16:82061000-82066800 Weak transcription Esophagus oesophagus

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