Variant report

Variant rs111960951
Chromosome Location chr6:35755389-35755390
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:35746400-35755400 Weak transcription Pancreas Pancrea
2 chr6:35754200-35755400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:35754400-35756000 Bivalent Enhancer Placenta Placenta
4 chr6:35754600-35755400 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
5 chr6:35754600-35755600 Bivalent Enhancer Liver Liver
6 chr6:35754800-35755600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr6:35754800-35755600 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
8 chr6:35755000-35755400 Bivalent Enhancer HepG2 liver
9 chr6:35755000-35755600 Bivalent Enhancer ES-WA7 Cell Line embryonic stem cell
10 chr6:35755000-35755600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
11 chr6:35755000-35756000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
12 chr6:35755200-35755400 Flanking Bivalent TSS/Enh ES-I3 Cell Line embryonic stem cell
13 chr6:35755200-35755400 Bivalent Enhancer H1 Cell Line embryonic stem cell
14 chr6:35755200-35755400 Bivalent Enhancer Duodenum Mucosa Duodenum
15 chr6:35755200-35756600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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