Variant report

Variant rs17223651
Chromosome Location chr12:76087932-76087933
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:76076200-76098400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr12:76079000-76093600 Weak transcription Psoas Muscle Psoas
3 chr12:76079400-76099800 Weak transcription Right Atrium heart
4 chr12:76084600-76088400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr12:76084600-76088400 Weak transcription K562 blood
6 chr12:76084600-76088600 Weak transcription A549 lung
7 chr12:76084600-76099600 Weak transcription Pancreas Pancrea
8 chr12:76086200-76093600 Weak transcription NHLF lung
9 chr12:76086400-76088200 Weak transcription HMEC breast
10 chr12:76086400-76088400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr12:76086800-76099400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr12:76087000-76088000 Weak transcription NHDF-Ad bronchial
13 chr12:76087000-76088800 Weak transcription Osteobl bone
14 chr12:76087400-76088400 Weak transcription Muscle Satellite Cultured Cells --
15 chr12:76087800-76088800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr12:76087800-76089600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr12:76087800-76089600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr12:76087800-76089600 Enhancers NHEK skin

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