Variant report

Variant rs548674437
Chromosome Location chr6:35755428-35755429
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:35754400-35756000 Bivalent Enhancer Placenta Placenta
2 chr6:35754600-35755600 Bivalent Enhancer Liver Liver
3 chr6:35754800-35755600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr6:35754800-35755600 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
5 chr6:35755000-35755600 Bivalent Enhancer ES-WA7 Cell Line embryonic stem cell
6 chr6:35755000-35755600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
7 chr6:35755000-35756000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
8 chr6:35755200-35756600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr6:35755400-35755800 Flanking Active TSS HepG2 liver
10 chr6:35755400-35757000 Enhancers Pancreas Pancrea
11 chr6:35755400-35765600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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