Variant report

Variant rs41289999
Chromosome Location chr9:140777162-140777163
allele G/T
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 chr9:140774000-140777200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr9:140776000-140777200 Weak transcription Spleen Spleen
4 chr9:140776200-140777200 Enhancers Brain Dorsolateral Prefrontal Cortex brain
5 chr9:140776400-140777200 Strong transcription Fetal Brain Female brain
6 chr9:140776800-140777200 Bivalent Enhancer Brain Cingulate Gyrus brain
7 chr9:140776800-140778800 ZNF genes & repeats H9 Cell Line embryonic stem cell
8 chr9:140777000-140777200 Genic enhancers Brain Germinal Matrix brain
9 chr9:140777000-140777400 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell
10 chr9:140777000-140777600 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
11 chr9:140777000-140777600 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
12 chr9:140777000-140777600 Flanking Bivalent TSS/Enh iPS DF 19.11 Cell Line embryonic stem cell
13 chr9:140777000-140778400 Bivalent Enhancer Brain Inferior Temporal Lobe brain
14 chr9:140777000-140779800 Bivalent Enhancer Fetal Brain Male brain

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