Variant report

Variant rs2041498
Chromosome Location chr2:37933006-37933007
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:37917200-37938000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:37917200-37938800 Weak transcription Aorta Aorta
3 chr2:37927000-37934200 Weak transcription Placenta Placenta
4 chr2:37927000-37937800 Weak transcription NHLF lung
5 chr2:37927200-37933400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr2:37932000-37934200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr2:37932200-37933400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr2:37932200-37934400 Enhancers Osteobl bone
9 chr2:37932200-37934600 Enhancers NHDF-Ad bronchial
10 chr2:37932400-37935400 Weak transcription Muscle Satellite Cultured Cells --
11 chr2:37932800-37934400 Enhancers Sigmoid Colon Sigmoid Colon
12 chr2:37932800-37935000 Enhancers Monocytes-CD14+_RO01746 blood
13 chr2:37932800-37936400 Enhancers Primary monocytes fromperipheralblood blood
14 chr2:37933000-37933400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
15 chr2:37933000-37934000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
16 chr2:37933000-37934400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
17 chr2:37933000-37934400 Enhancers Lung lung
18 chr2:37933000-37934800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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