Variant report

Variant rs17014956
Chromosome Location chr2:34467939-34467940
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:34465600-34468400 Enhancers Ovary ovary
2 chr2:34465800-34468000 Enhancers Fetal Kidney kidney
3 chr2:34466400-34468200 Enhancers Pancreas Pancrea
4 chr2:34466400-34468400 Enhancers Fetal Lung lung
5 chr2:34466400-34468600 Enhancers Fetal Brain Male brain
6 chr2:34466600-34468600 Enhancers Liver Liver
7 chr2:34467000-34468200 Enhancers Brain Germinal Matrix brain
8 chr2:34467000-34468600 Enhancers Fetal Intestine Large intestine
9 chr2:34467000-34468600 Enhancers Fetal Intestine Small intestine
10 chr2:34467000-34468600 Enhancers Rectal Mucosa Donor 31 rectum
11 chr2:34467200-34468000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr2:34467200-34468200 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
13 chr2:34467200-34468400 Enhancers Duodenum Mucosa Duodenum
14 chr2:34467400-34468000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
15 chr2:34467400-34468200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr2:34467400-34475600 Weak transcription Rectal Mucosa Donor 29 rectum
17 chr2:34467600-34469200 Weak transcription Pancreatic Islets Pancreatic Islet

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