Variant report

Variant rs8105094
Chromosome Location chr19:19374061-19374062
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:19371800-19374200 Flanking Active TSS iPS DF 19.11 Cell Line embryonic stem cell
2 chr19:19373000-19384000 Weak transcription Pancreas Pancrea
3 chr19:19373200-19374200 Bivalent/Poised TSS iPS-18 Cell Line embryonic stem cell
4 chr19:19373200-19375000 Weak transcription Liver Liver
5 chr19:19373800-19374200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
6 chr19:19373800-19374400 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
7 chr19:19374000-19374200 Bivalent Enhancer H1 Cell Line embryonic stem cell
8 chr19:19374000-19374200 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
9 chr19:19374000-19374200 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
10 chr19:19374000-19374200 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
11 chr19:19374000-19374200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
12 chr19:19374000-19374600 Weak transcription Brain Angular Gyrus brain
13 chr19:19374000-19383400 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr19:19374000-19383400 Weak transcription Right Atrium heart

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