Variant report

Variant rs138618211
Chromosome Location chr9:140779722-140779723
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:140773200-140795400 Weak transcription Right Atrium heart
2 chr9:140777000-140779800 Bivalent Enhancer Fetal Brain Male brain
3 chr9:140777200-140780200 Bivalent Enhancer Fetal Brain Female brain
4 chr9:140777200-140782000 ZNF genes & repeats Spleen Spleen
5 chr9:140777600-140787200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
6 chr9:140778600-140787000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr9:140778800-140780400 Bivalent Enhancer Brain Germinal Matrix brain
8 chr9:140779000-140780000 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr9:140779000-140780200 Bivalent/Poised TSS Brain Dorsolateral Prefrontal Cortex brain
10 chr9:140779200-140780800 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr9:140779200-140785000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr9:140779400-140780200 Bivalent Enhancer Esophagus oesophagus
13 chr9:140779600-140779800 Flanking Bivalent TSS/Enh H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr9:140779600-140779800 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
15 chr9:140779600-140779800 Flanking Bivalent TSS/Enh Brain Cingulate Gyrus brain
16 chr9:140779600-140780200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin

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