Variant report

Variant rs369202674
Chromosome Location chr16:82060805-82060806
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:82057200-82061000 Weak transcription Stomach Mucosa stomach
2 chr16:82058000-82065600 Weak transcription Gastric stomach
3 chr16:82058600-82062400 Enhancers Duodenum Mucosa Duodenum
4 chr16:82059400-82062200 Enhancers Fetal Intestine Large intestine
5 chr16:82060000-82062000 Enhancers Fetal Intestine Small intestine
6 chr16:82060600-82061800 Weak transcription Small Intestine intestine
7 chr16:82060600-82062000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr16:82060600-82062200 Enhancers NHEK skin
9 chr16:82060800-82061000 Enhancers Esophagus oesophagus
10 chr16:82060800-82061000 Enhancers Pancreas Pancrea
11 chr16:82060800-82061400 Enhancers HMEC breast
12 chr16:82060800-82062000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr16:82060800-82062200 Enhancers Liver Liver

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