Variant report

Variant rs198973
Chromosome Location chr19:51380525-51380526
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:51378200-51380600 Enhancers Primary B cells from peripheral blood blood
2 chr19:51379800-51380600 Enhancers GM12878-XiMat blood
3 chr19:51379800-51380800 Bivalent Enhancer Sigmoid Colon Sigmoid Colon
4 chr19:51380000-51380600 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
5 chr19:51380000-51380600 Bivalent Enhancer H1 Cell Line embryonic stem cell
6 chr19:51380000-51381400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr19:51380200-51380800 Enhancers ES-WA7 Cell Line embryonic stem cell
8 chr19:51380400-51380600 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell
9 chr19:51380400-51381000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
10 chr19:51380400-51381200 Enhancers ES-UCSF4 Cell Line embryonic stem cell

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