Variant report

Variant rs13239462
Chromosome Location chr7:17048217-17048218
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr7:17045800-17048800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr7:17047800-17052400 Weak transcription Osteobl bone
9 chr7:17048000-17049400 Weak transcription HMEC breast
10 chr7:17048000-17049600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr7:17048200-17048600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr7:17048200-17048600 Enhancers Monocytes-CD14+_RO01746 blood
13 chr7:17048200-17050400 Weak transcription NHEK skin

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