Variant report

Variant rs577758515
Chromosome Location chr9:140779954-140779955
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 chr9:140777200-140780200 Bivalent Enhancer Fetal Brain Female brain
3 chr9:140777200-140782000 ZNF genes & repeats Spleen Spleen
4 chr9:140777600-140787200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
5 chr9:140778600-140787000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr9:140778800-140780400 Bivalent Enhancer Brain Germinal Matrix brain
7 chr9:140779000-140780000 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr9:140779000-140780200 Bivalent/Poised TSS Brain Dorsolateral Prefrontal Cortex brain
9 chr9:140779200-140780800 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chr9:140779200-140785000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr9:140779400-140780200 Bivalent Enhancer Esophagus oesophagus
12 chr9:140779600-140780200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
13 chr9:140779800-140780200 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr9:140779800-140780200 Bivalent Enhancer Brain Cingulate Gyrus brain

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