Variant report

Variant rs73656784
Chromosome Location chr9:118393619-118393620
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:118385000-118394800 Weak transcription Aorta Aorta
2 chr9:118387800-118395200 Weak transcription HSMM muscle
3 chr9:118390600-118395000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr9:118390800-118394800 Weak transcription NH-A brain
5 chr9:118390800-118398800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr9:118391000-118395200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr9:118391200-118394800 Weak transcription NHEK skin
8 chr9:118392600-118395200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr9:118392600-118395200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr9:118392600-118395200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr9:118392800-118395200 Weak transcription Osteobl bone
12 chr9:118393000-118394600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr9:118393400-118395000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr9:118393400-118395000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
15 chr9:118393400-118399800 Weak transcription NHLF lung
16 chr9:118393600-118395200 Weak transcription NHDF-Ad bronchial

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