Variant report

Variant rs10230578
Chromosome Location chr7:27290360-27290361
allele A/T
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 chr7:27288400-27292200 Bivalent Enhancer Primary B cells from peripheral blood blood
6 chr7:27289000-27290800 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
7 chr7:27289000-27291000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
8 chr7:27289000-27292000 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr7:27289800-27290800 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
10 chr7:27290000-27290600 Bivalent Enhancer hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr7:27290200-27290400 Bivalent Enhancer Primary T helper memory cells from peripheral blood 2 blood
12 chr7:27290200-27290600 Bivalent Enhancer Brain Germinal Matrix brain
13 chr7:27290200-27290800 Bivalent Enhancer Skeletal Muscle Female skeletal muscle

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