Variant report

Variant rs7007937
Chromosome Location chr8:49661247-49661248
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49656800-49662400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr8:49659200-49661400 Enhancers Fetal Lung lung
3 chr8:49660000-49661600 Enhancers NHLF lung
4 chr8:49660200-49661600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
5 chr8:49660200-49661800 Enhancers NHDF-Ad bronchial
6 chr8:49660400-49662400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr8:49660800-49661400 Enhancers HSMM muscle
8 chr8:49660800-49661400 Enhancers HSMMtube muscle
9 chr8:49660800-49661600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr8:49660800-49661600 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr8:49660800-49661600 Enhancers Osteobl bone
12 chr8:49661000-49661400 Enhancers Muscle Satellite Cultured Cells --
13 chr8:49661000-49668200 Weak transcription Pancreas Pancrea
14 chr8:49661200-49661800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr8:49661200-49662400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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