Variant report

Variant rs36092492
Chromosome Location chr9:802389-802390
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:794600-809600 Weak transcription Right Atrium heart
2 chr9:800400-802400 Enhancers Cortex derived primary cultured neurospheres brain
3 chr9:800600-802800 Enhancers NH-A brain
4 chr9:801200-802400 Enhancers Muscle Satellite Cultured Cells --
5 chr9:801200-802400 Enhancers Fetal Kidney kidney
6 chr9:801200-802400 Enhancers Osteobl bone
7 chr9:801400-802400 Flanking Active TSS NHEK skin
8 chr9:801400-802800 Enhancers HMEC breast
9 chr9:801400-803600 Flanking Active TSS HUVEC blood vessel
10 chr9:801600-802600 Enhancers HUES64 Cell Line embryonic stem cell
11 chr9:801800-802400 Weak transcription Hela-S3 cervix
12 chr9:802000-802400 Flanking Active TSS IMR90 fetal lung fibroblasts Cell Line lung
13 chr9:802000-802400 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
14 chr9:802000-802400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr9:802000-802400 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr9:802000-802400 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr9:802000-802600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
18 chr9:802200-805000 Weak transcription ES-I3 Cell Line embryonic stem cell

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