Variant report

Variant rs12078145
Chromosome Location chr1:193247765-193247766
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:193218600-193258200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr1:193222400-193253800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr1:193229000-193254800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr1:193231600-193251200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr1:193232000-193249400 Weak transcription Fetal Heart heart
6 chr1:193235400-193252000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr1:193235400-193252200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr1:193239800-193254600 Weak transcription HSMM muscle
9 chr1:193241000-193251800 Weak transcription Muscle Satellite Cultured Cells --
10 chr1:193243800-193250000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr1:193243800-193254400 Weak transcription HSMMtube muscle
12 chr1:193243800-193267800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:193245000-193252000 Weak transcription HUES48 Cell Line embryonic stem cell
14 chr1:193245400-193253200 Weak transcription Primary T cells from cord blood blood

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