Variant report

Variant rs113170757
Chromosome Location chr9:140783505-140783506
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:140773200-140795400 Weak transcription Right Atrium heart
2 chr9:140777600-140787200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
3 chr9:140778600-140787000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr9:140779200-140785000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr9:140781600-140783800 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr9:140782000-140785400 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr9:140782400-140784000 Strong transcription Brain Germinal Matrix brain
8 chr9:140782800-140783600 Weak transcription Spleen Spleen
9 chr9:140783200-140783600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
10 chr9:140783200-140784200 Enhancers Fetal Thymus thymus
11 chr9:140783200-140785600 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
12 chr9:140783400-140783600 Bivalent Enhancer Brain Anterior Caudate brain
13 chr9:140783400-140783800 Transcr. at gene 5' and 3' iPS DF 19.11 Cell Line embryonic stem cell
14 chr9:140783400-140783800 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast

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