Variant report

Variant rs3919529
Chromosome Location chr7:17664424-17664425
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17662800-17665200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
2 chr7:17662800-17666000 Enhancers Hela-S3 cervix
3 chr7:17663000-17665000 Enhancers Muscle Satellite Cultured Cells --
4 chr7:17663000-17666600 Enhancers NHDF-Ad bronchial
5 chr7:17663200-17664600 Enhancers NH-A brain
6 chr7:17663200-17665200 Enhancers HSMM muscle
7 chr7:17663200-17665600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr7:17663200-17665800 Enhancers Osteobl bone
9 chr7:17663200-17666200 Enhancers NHLF lung
10 chr7:17663200-17666400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr7:17663400-17664600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
12 chr7:17663600-17665000 Enhancers A549 lung
13 chr7:17663800-17666000 Enhancers HMEC breast
14 chr7:17664000-17665600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr7:17664200-17665000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr7:17664200-17665200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
17 chr7:17664200-17665200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
18 chr7:17664400-17665600 Enhancers NHEK skin

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