Variant report

Variant rs7937176
Chromosome Location chr11:17279745-17279746
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:17278000-17280400 Enhancers A549 lung
2 chr11:17278400-17279800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr11:17278600-17279800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr11:17278600-17280200 Enhancers K562 blood
5 chr11:17278600-17280600 Enhancers Stomach Mucosa stomach
6 chr11:17278800-17280000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr11:17278800-17280000 Enhancers Rectal Mucosa Donor 31 rectum
8 chr11:17278800-17281000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr11:17278800-17288800 Weak transcription Placenta Placenta
10 chr11:17279000-17280000 Enhancers Muscle Satellite Cultured Cells --
11 chr11:17279000-17280000 Enhancers Hela-S3 cervix
12 chr11:17279000-17281000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr11:17279000-17281000 Weak transcription NHEK skin
14 chr11:17279000-17281200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr11:17279000-17284600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
16 chr11:17279000-17284600 Weak transcription NHLF lung
17 chr11:17279000-17284800 Weak transcription HMEC breast
18 chr11:17279200-17284600 Weak transcription Osteobl bone
19 chr11:17279400-17280400 Weak transcription Placenta Amnion Placenta Amnion
20 chr11:17279600-17280600 Enhancers HepG2 liver

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