Variant report

Variant rs72915043
Chromosome Location chr4:100889067-100889068
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:100880400-100889600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr4:100882800-100892800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr4:100887000-100890000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr4:100887800-100889800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr4:100887800-100890200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr4:100888400-100889400 Weak transcription NHLF lung
7 chr4:100888400-100890200 Enhancers Muscle Satellite Cultured Cells --
8 chr4:100888400-100890400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr4:100888800-100889200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr4:100888800-100893200 Weak transcription Right Ventricle heart
11 chr4:100889000-100889400 Enhancers NH-A brain
12 chr4:100889000-100889800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr4:100889000-100890200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr4:100889000-100890200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr4:100889000-100890200 Enhancers HSMMtube muscle
16 chr4:100889000-100890200 Enhancers NHDF-Ad bronchial
17 chr4:100889000-100890200 Enhancers NHEK skin
18 chr4:100889000-100890200 Enhancers Osteobl bone

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