Variant report

Variant rs11901908
Chromosome Location chr2:114744174-114744175
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:114734000-114746000 Weak transcription Aorta Aorta
2 chr2:114734000-114751800 Weak transcription Primary mononuclear cells fromperipheralblood Blood
3 chr2:114734400-114749800 Weak transcription Primary T cells fromperipheralblood blood
4 chr2:114736200-114761000 Weak transcription HSMMtube muscle
5 chr2:114737400-114746000 Weak transcription Primary neutrophils fromperipheralblood blood
6 chr2:114737600-114751400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr2:114737800-114754400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
8 chr2:114738000-114744600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr2:114738000-114748800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr2:114738600-114749400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr2:114739200-114744600 Weak transcription NHDF-Ad bronchial
12 chr2:114739600-114752600 Weak transcription NH-A brain
13 chr2:114740600-114745200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr2:114741200-114761000 Weak transcription HSMM muscle
15 chr2:114742200-114746200 Enhancers HepG2 liver
16 chr2:114743000-114751000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
17 chr2:114743800-114745600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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