Variant report

Variant rs35703856
Chromosome Location chr7:17139501-17139502
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17133400-17140000 Enhancers HMEC breast
2 chr7:17133800-17139800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr7:17137400-17139600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:17137400-17139600 Flanking Active TSS Liver Liver
5 chr7:17137400-17140000 Enhancers Rectal Mucosa Donor 31 rectum
6 chr7:17138000-17139600 Enhancers Esophagus oesophagus
7 chr7:17138000-17139600 Enhancers NHEK skin
8 chr7:17138000-17140800 Enhancers HepG2 liver
9 chr7:17138200-17139600 Enhancers Fetal Intestine Small intestine
10 chr7:17138400-17140400 Enhancers Stomach Mucosa stomach
11 chr7:17138600-17139600 Enhancers Fetal Intestine Large intestine
12 chr7:17139000-17139600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr7:17139000-17139600 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr7:17139000-17139600 Enhancers Placenta Placenta
15 chr7:17139000-17139600 Enhancers Lung lung
16 chr7:17139200-17139600 Enhancers Gastric stomach
17 chr7:17139200-17140200 Enhancers Hela-S3 cervix
18 chr7:17139400-17139800 Enhancers Pancreas Pancrea
19 chr7:17139400-17140400 Enhancers A549 lung

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