Variant report

Variant rs148176685
Chromosome Location chr15:76870499-76870500
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:26 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:76862600-76872000 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
2 chr15:76868400-76870800 Enhancers Esophagus oesophagus
3 chr15:76868400-76871000 Enhancers Ovary ovary
4 chr15:76868600-76870800 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr15:76868800-76870600 Enhancers Skeletal Muscle Male skeletal muscle
6 chr15:76868800-76870800 Enhancers Right Atrium heart
7 chr15:76868800-76871000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr15:76868800-76871200 Enhancers NHEK skin
9 chr15:76869000-76870800 Enhancers Aorta Aorta
10 chr15:76869000-76870800 Enhancers Left Ventricle heart
11 chr15:76869000-76870800 Enhancers Rectal Mucosa Donor 31 rectum
12 chr15:76869000-76870800 Enhancers HepG2 liver
13 chr15:76869000-76870800 Enhancers HMEC breast
14 chr15:76869000-76871000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr15:76869400-76870600 Weak transcription Fetal Thymus thymus
16 chr15:76869400-76881200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr15:76869600-76870600 Enhancers Duodenum Mucosa Duodenum
18 chr15:76869800-76870600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
19 chr15:76869800-76870600 Enhancers Hela-S3 cervix
20 chr15:76870000-76871000 Strong transcription Fetal Intestine Small intestine
21 chr15:76870000-76871800 Weak transcription Fetal Intestine Large intestine
22 chr15:76870200-76870800 Enhancers Primary Natural Killer cells fromperipheralblood blood
23 chr15:76870200-76872600 Weak transcription Brain Substantia Nigra brain
24 chr15:76870400-76872000 Weak transcription Spleen Spleen
25 chr15:76870400-76876000 Weak transcription Right Ventricle heart
26 chr15:76870400-76881200 Weak transcription Lung lung

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