Variant report

Variant rs73683614
Chromosome Location chr7:17047618-17047619
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17033400-17052600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr7:17043800-17048600 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr7:17045600-17048400 Weak transcription Primary monocytes fromperipheralblood blood
4 chr7:17045600-17049200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr7:17045600-17049200 Weak transcription Adipose Nuclei Adipose
6 chr7:17045600-17056200 Weak transcription Stomach Mucosa stomach
7 chr7:17045800-17048200 Weak transcription Monocytes-CD14+_RO01746 blood
8 chr7:17045800-17048800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr7:17047200-17048000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr7:17047200-17048000 Enhancers HMEC breast
11 chr7:17047400-17047800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr7:17047400-17047800 Enhancers Osteobl bone
13 chr7:17047400-17048000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr7:17047400-17048200 Enhancers NHEK skin
15 chr7:17047600-17047800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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