Variant report

Variant rs6988916
Chromosome Location chr8:49660909-49660910
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49648600-49661000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr8:49656800-49662400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr8:49659200-49661400 Enhancers Fetal Lung lung
4 chr8:49660000-49661600 Enhancers NHLF lung
5 chr8:49660200-49661000 Enhancers Pancreas Pancrea
6 chr8:49660200-49661200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
7 chr8:49660200-49661600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr8:49660200-49661800 Enhancers NHDF-Ad bronchial
9 chr8:49660400-49661000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr8:49660400-49662400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
11 chr8:49660800-49661400 Enhancers HSMM muscle
12 chr8:49660800-49661400 Enhancers HSMMtube muscle
13 chr8:49660800-49661600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr8:49660800-49661600 Enhancers Fetal Adrenal Gland Adrenal Gland
15 chr8:49660800-49661600 Enhancers Osteobl bone

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