Variant report

Variant rs2101686
Chromosome Location chr9:72488177-72488178
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr9:72486800-72488400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr9:72486800-72488800 Weak transcription NHDF-Ad bronchial
5 chr9:72487000-72488200 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr9:72487000-72488600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr9:72487400-72490000 Enhancers HUES6 Cell Line embryonic stem cell
8 chr9:72487600-72488400 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr9:72487600-72489200 Enhancers Psoas Muscle Psoas
10 chr9:72487600-72489600 Weak transcription iPS-18 Cell Line embryonic stem cell
11 chr9:72487800-72490600 Enhancers Fetal Heart heart
12 chr9:72488000-72488400 Enhancers Skeletal Muscle Male skeletal muscle
13 chr9:72488000-72488600 Enhancers Skeletal Muscle Female skeletal muscle

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