Variant report

Variant rs28357175
Chromosome Location chr7:27288235-27288236
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:27283600-27293600 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
2 chr7:27286000-27291200 Weak transcription Gastric stomach
3 chr7:27286200-27291000 Weak transcription Right Atrium heart
4 chr7:27286200-27291200 Weak transcription Pancreas Pancrea
5 chr7:27287800-27288800 Enhancers HMEC breast
6 chr7:27288000-27288400 Bivalent Enhancer H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr7:27288200-27288400 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
8 chr7:27288200-27288600 Bivalent Enhancer NHEK skin
9 chr7:27288200-27288800 Bivalent Enhancer HSMM muscle
10 chr7:27288200-27289000 Bivalent Enhancer Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr7:27288200-27289000 Bivalent Enhancer HSMMtube muscle
12 chr7:27288200-27289000 Bivalent Enhancer Osteobl bone
13 chr7:27288200-27289400 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr7:27288200-27289600 Bivalent Enhancer Primary monocytes fromperipheralblood blood

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