Variant report

Variant rs17501898
Chromosome Location chr7:27289410-27289411
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr7:27288200-27289600 Bivalent Enhancer Primary monocytes fromperipheralblood blood
6 chr7:27288400-27292200 Bivalent Enhancer Primary B cells from peripheral blood blood
7 chr7:27289000-27290000 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
8 chr7:27289000-27290800 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
9 chr7:27289000-27291000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
10 chr7:27289000-27292000 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr7:27289200-27289600 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
12 chr7:27289400-27289600 Bivalent Enhancer Primary T helper cells fromperipheralblood blood
13 chr7:27289400-27289800 Bivalent Enhancer hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived

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