Variant report

Variant rs2678136
Chromosome Location chr12:43188032-43188033
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:43185200-43188200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr12:43185200-43188400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr12:43185200-43188400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr12:43185200-43193000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr12:43185400-43188200 Weak transcription Fetal Heart heart
6 chr12:43185400-43188200 Weak transcription A549 lung
7 chr12:43185400-43188200 Weak transcription HMEC breast
8 chr12:43185400-43188200 Weak transcription Osteobl bone
9 chr12:43185400-43188400 Weak transcription NH-A brain
10 chr12:43185400-43192200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr12:43185400-43192200 Weak transcription HSMMtube muscle
12 chr12:43188000-43188200 Enhancers Placenta Placenta
13 chr12:43188000-43188200 Enhancers HSMM muscle
14 chr12:43188000-43188600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr12:43188000-43189200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr12:43188000-43189200 Enhancers Muscle Satellite Cultured Cells --
17 chr12:43188000-43189200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
18 chr12:43188000-43189200 Enhancers NHDF-Ad bronchial

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