Variant report

Variant rs111333558
Chromosome Location chr9:140780020-140780021
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr9:140779000-140780200 Bivalent/Poised TSS Brain Dorsolateral Prefrontal Cortex brain
8 chr9:140779200-140780800 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr9:140779200-140785000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr9:140779400-140780200 Bivalent Enhancer Esophagus oesophagus
11 chr9:140779600-140780200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
12 chr9:140779800-140780200 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr9:140779800-140780200 Bivalent Enhancer Brain Cingulate Gyrus brain
14 chr9:140780000-140780200 Bivalent Enhancer Fetal Muscle Trunk muscle
15 chr9:140780000-140780600 Transcr. at gene 5' and 3' iPS DF 19.11 Cell Line embryonic stem cell

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