Variant report

Variant rs10864142
Chromosome Location chr1:215165561-215165562
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:215163800-215166800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:215163800-215168200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr1:215164000-215166800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr1:215164200-215166800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:215164200-215166800 Weak transcription NHLF lung
6 chr1:215164200-215167800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr1:215164200-215174800 Weak transcription NH-A brain
8 chr1:215164400-215166600 Weak transcription NHEK skin
9 chr1:215164800-215166800 Weak transcription HMEC breast
10 chr1:215164800-215166800 Weak transcription Osteobl bone
11 chr1:215164800-215167000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr1:215164800-215175000 Weak transcription Muscle Satellite Cultured Cells --
13 chr1:215165200-215166600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr1:215165200-215166600 Weak transcription NHDF-Ad bronchial
15 chr1:215165200-215166800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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