Variant report

Variant rs4742415
Chromosome Location chr9:801706-801707
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:794600-809600 Weak transcription Right Atrium heart
2 chr9:800400-802000 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr9:800400-802400 Enhancers Cortex derived primary cultured neurospheres brain
4 chr9:800600-802800 Enhancers NH-A brain
5 chr9:801000-801800 Enhancers Hela-S3 cervix
6 chr9:801000-802000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr9:801200-802400 Enhancers Muscle Satellite Cultured Cells --
8 chr9:801200-802400 Enhancers Fetal Kidney kidney
9 chr9:801200-802400 Enhancers Osteobl bone
10 chr9:801400-802200 Enhancers ES-WA7 Cell Line embryonic stem cell
11 chr9:801400-802400 Flanking Active TSS NHEK skin
12 chr9:801400-802800 Enhancers HMEC breast
13 chr9:801400-803600 Flanking Active TSS HUVEC blood vessel
14 chr9:801600-801800 Enhancers Duodenum Mucosa Duodenum
15 chr9:801600-802000 Active TSS IMR90 fetal lung fibroblasts Cell Line lung
16 chr9:801600-802000 Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr9:801600-802000 Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr9:801600-802200 Enhancers ES-I3 Cell Line embryonic stem cell
19 chr9:801600-802600 Enhancers HUES64 Cell Line embryonic stem cell

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