Variant report

Variant rs537873756
Chromosome Location chr6:35755851-35755852
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:35754400-35756000 Bivalent Enhancer Placenta Placenta
2 chr6:35755000-35756000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
3 chr6:35755200-35756600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr6:35755400-35757000 Enhancers Pancreas Pancrea
5 chr6:35755400-35765600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr6:35755600-35756000 Enhancers Liver Liver
7 chr6:35755600-35758600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr6:35755800-35756400 Enhancers HepG2 liver

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