Variant report

Variant rs185969558
Chromosome Location chr4:69521525-69521526
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:69513000-69522800 Weak transcription Pancreas Pancrea
2 chr4:69516600-69521800 Strong transcription Liver Liver
3 chr4:69519800-69522200 Enhancers NHEK skin
4 chr4:69519800-69523000 Enhancers HMEC breast
5 chr4:69520400-69521800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr4:69520400-69523000 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr4:69520400-69523000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr4:69520800-69521800 Enhancers A549 lung
9 chr4:69520800-69521800 Enhancers HepG2 liver
10 chr4:69521000-69522600 Enhancers HUES6 Cell Line embryonic stem cell
11 chr4:69521200-69521600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr4:69521200-69522600 Enhancers Rectal Mucosa Donor 31 rectum
13 chr4:69521200-69522600 Enhancers Stomach Mucosa stomach
14 chr4:69521200-69522800 Enhancers H9 Cell Line embryonic stem cell
15 chr4:69521200-69522800 Enhancers HUES48 Cell Line embryonic stem cell
16 chr4:69521200-69522800 Enhancers Fetal Intestine Large intestine
17 chr4:69521400-69522200 Enhancers iPS-18 Cell Line embryonic stem cell
18 chr4:69521400-69522800 Enhancers iPS-15b Cell Line embryonic stem cell

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