Variant report

Variant rs7858907
Chromosome Location chr9:72980674-72980675
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:72944000-73002600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr9:72948000-72983400 Weak transcription HSMMtube muscle
3 chr9:72948400-72980800 Weak transcription NHEK skin
4 chr9:72964200-72980800 Weak transcription Pancreas Pancrea
5 chr9:72966600-72983000 Weak transcription NHDF-Ad bronchial
6 chr9:72967400-72989600 Weak transcription Muscle Satellite Cultured Cells --
7 chr9:72969000-72982800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr9:72971200-72982200 Weak transcription Psoas Muscle Psoas
9 chr9:72972800-72981000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr9:72972800-72982800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
11 chr9:72972800-73002400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
12 chr9:72973200-72989600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr9:72973800-72988800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr9:72978200-73001000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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