Variant report

Variant rs3008732
Chromosome Location chr9:16001924-16001925
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:15999000-16003200 Enhancers NHDF-Ad bronchial
2 chr9:15999000-16003600 Enhancers HMEC breast
3 chr9:15999400-16002400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr9:15999400-16002400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr9:15999400-16002800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr9:15999800-16003600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr9:15999800-16003600 Enhancers Osteobl bone
8 chr9:15999800-16003800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr9:16000200-16002800 Enhancers NH-A brain
10 chr9:16000200-16003600 Enhancers Muscle Satellite Cultured Cells --
11 chr9:16000200-16010400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
12 chr9:16000600-16003800 Weak transcription HSMM muscle
13 chr9:16000800-16002800 Weak transcription A549 lung
14 chr9:16001200-16002200 Weak transcription NHLF lung
15 chr9:16001600-16002000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr9:16001600-16011800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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