The 2.0 version of rSNPBase

Variant report

Variant esv2645018
Chromosome Location chr8:107601275-107601278
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:107512400-107620200 Weak transcription Aorta Aorta
2 chr8:107590200-107601400 Weak transcription Pancreas Pancrea
3 chr8:107592400-107606600 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr8:107600600-107601800 Enhancers Fetal Intestine Large intestine
5 chr8:107600800-107601800 Enhancers Fetal Intestine Small intestine
6 chr8:107601200-107601400 Genic enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr8:107601200-107601400 Flanking Active TSS A549 lung
8 chr8:107601200-107601400 Enhancers HepG2 liver
9 chr8:107601200-107601600 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr8:107601200-107601600 Flanking Active TSS Duodenum Mucosa Duodenum
11 chr8:107601200-107601600 Enhancers Gastric stomach
12 chr8:107601200-107601600 Enhancers Stomach Mucosa stomach
13 chr8:107601200-107602000 Enhancers Rectal Mucosa Donor 29 rectum
14 chr8:107601200-107602000 Enhancers Rectal Mucosa Donor 31 rectum
15 chr8:107601200-107602200 Enhancers Fetal Adrenal Gland Adrenal Gland

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Last update: Aug 31, 2015