Variant report

Variant rs57477899
Chromosome Location chr9:72488622-72488623
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:72475400-72495200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr9:72476200-72492800 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr9:72486800-72488800 Weak transcription NHDF-Ad bronchial
4 chr9:72487400-72490000 Enhancers HUES6 Cell Line embryonic stem cell
5 chr9:72487600-72489200 Enhancers Psoas Muscle Psoas
6 chr9:72487600-72489600 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr9:72487800-72490600 Enhancers Fetal Heart heart
8 chr9:72488200-72488800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr9:72488200-72492400 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chr9:72488400-72489000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr9:72488400-72489000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
12 chr9:72488400-72489400 Flanking Active TSS Skeletal Muscle Male skeletal muscle
13 chr9:72488400-72492600 Weak transcription iPS-20b Cell Line embryonic stem cell
14 chr9:72488600-72489000 Flanking Active TSS Skeletal Muscle Female skeletal muscle
15 chr9:72488600-72489200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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