Variant report

Variant rs55914832
Chromosome Location chr3:160996179-160996180
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:160972200-160996600 Weak transcription Brain Substantia Nigra brain
2 chr3:160979200-160999800 Weak transcription Psoas Muscle Psoas
3 chr3:160982400-160996600 Weak transcription Adipose Nuclei Adipose
4 chr3:160984800-161002400 Weak transcription NHEK skin
5 chr3:160985200-160996600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr3:160988000-160996200 Weak transcription Brain Hippocampus Middle brain
7 chr3:160989000-161000400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr3:160994400-160996800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr3:160994400-160997600 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr3:160994400-160997600 Weak transcription Left Ventricle heart
11 chr3:160994600-161002200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr3:160994600-161016800 Weak transcription Right Ventricle heart
13 chr3:160994800-160996600 Weak transcription HSMM muscle
14 chr3:160995200-160996800 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
15 chr3:160995400-160996200 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell

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