Variant report

Variant rs569463836
Chromosome Location chr6:35755092-35755093
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 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 chr6:35754400-35755200 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr6:35754400-35756000 Bivalent Enhancer Placenta Placenta
5 chr6:35754600-35755200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr6:35754600-35755200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
7 chr6:35754600-35755200 Flanking Bivalent TSS/Enh Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr6:35754600-35755200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
9 chr6:35754600-35755400 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
10 chr6:35754600-35755600 Bivalent Enhancer Liver Liver
11 chr6:35754800-35755200 Bivalent Enhancer Lung lung
12 chr6:35754800-35755600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr6:35754800-35755600 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
14 chr6:35755000-35755200 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
15 chr6:35755000-35755200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
16 chr6:35755000-35755200 Bivalent/Poised TSS Duodenum Mucosa Duodenum
17 chr6:35755000-35755200 Bivalent Enhancer A549 lung
18 chr6:35755000-35755200 Bivalent Enhancer HMEC breast
19 chr6:35755000-35755400 Bivalent Enhancer HepG2 liver
20 chr6:35755000-35755600 Bivalent Enhancer ES-WA7 Cell Line embryonic stem cell
21 chr6:35755000-35755600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
22 chr6:35755000-35756000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin

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