Variant report

Variant rs886338
Chromosome Location chr7:27280455-27280456
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:27276000-27282000 Weak transcription Pancreas Pancrea
2 chr7:27278200-27281400 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
3 chr7:27278400-27282800 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
4 chr7:27278600-27282600 Bivalent Enhancer H1 Cell Line embryonic stem cell
5 chr7:27278800-27285000 Active TSS H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr7:27279400-27280600 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
7 chr7:27279400-27280600 Bivalent Enhancer Primary T killer naive cells fromperipheralblood blood
8 chr7:27279600-27280600 Active TSS hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr7:27279600-27280600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
10 chr7:27279600-27282200 Bivalent Enhancer H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr7:27279800-27281200 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
12 chr7:27279800-27282400 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
13 chr7:27280000-27285600 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell
14 chr7:27280200-27280600 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
15 chr7:27280200-27281200 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
16 chr7:27280400-27280800 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell

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