Variant report

Variant rs17090808
Chromosome Location chr1:71551145-71551146
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:71547600-71551400 Weak transcription Muscle Satellite Cultured Cells --
2 chr1:71547600-71551600 Weak transcription HSMMtube muscle
3 chr1:71547600-71551600 Weak transcription NHDF-Ad bronchial
4 chr1:71547600-71551800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:71547600-71555200 Weak transcription Lung lung
6 chr1:71547600-71555800 Weak transcription NHLF lung
7 chr1:71547800-71551200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr1:71547800-71551400 Weak transcription NHEK skin
9 chr1:71547800-71551600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr1:71547800-71551600 Weak transcription Fetal Intestine Small intestine
11 chr1:71547800-71551600 Weak transcription HSMM muscle
12 chr1:71547800-71551800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr1:71547800-71551800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr1:71547800-71551800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr1:71547800-71554600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr1:71549600-71555200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
17 chr1:71550800-71553400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
18 chr1:71551000-71551400 Genic enhancers Spleen Spleen
19 chr1:71551000-71552000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung

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