Variant report

Variant rs10815717
Chromosome Location chr9:801571-801572
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:794600-809600 Weak transcription Right Atrium heart
2 chr9:800400-801600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
3 chr9:800400-802000 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr9:800400-802400 Enhancers Cortex derived primary cultured neurospheres brain
5 chr9:800600-802800 Enhancers NH-A brain
6 chr9:801000-801600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr9:801000-801800 Enhancers Hela-S3 cervix
8 chr9:801000-802000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr9:801200-802400 Enhancers Muscle Satellite Cultured Cells --
10 chr9:801200-802400 Enhancers Fetal Kidney kidney
11 chr9:801200-802400 Enhancers Osteobl bone
12 chr9:801400-801600 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr9:801400-801600 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr9:801400-802200 Enhancers ES-WA7 Cell Line embryonic stem cell
15 chr9:801400-802400 Flanking Active TSS NHEK skin
16 chr9:801400-802800 Enhancers HMEC breast
17 chr9:801400-803600 Flanking Active TSS HUVEC blood vessel

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