Variant report

Variant rs17161615
Chromosome Location chr7:98793388-98793389
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:98791200-98793400 Weak transcription HepG2 liver
2 chr7:98792000-98793600 Weak transcription Muscle Satellite Cultured Cells --
3 chr7:98792200-98793400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr7:98792200-98793600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr7:98792200-98793600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr7:98792200-98793600 Weak transcription NH-A brain
7 chr7:98792200-98793600 Weak transcription Osteobl bone
8 chr7:98792200-98793800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr7:98792200-98794200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr7:98792200-98803600 Weak transcription Stomach Mucosa stomach
11 chr7:98792400-98793400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr7:98792400-98793400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr7:98792400-98793400 Weak transcription HMEC breast
14 chr7:98792400-98793400 Weak transcription NHEK skin
15 chr7:98792400-98793800 Weak transcription NHDF-Ad bronchial

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