Variant report

Variant rs2062808
Chromosome Location chr11:104981936-104981937
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:104975000-104983400 Weak transcription H9 Cell Line embryonic stem cell
2 chr11:104979000-104982600 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr11:104980200-104982200 Enhancers Cortex derived primary cultured neurospheres brain
4 chr11:104980600-104982000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
5 chr11:104981200-104982000 Enhancers Primary monocytes fromperipheralblood blood
6 chr11:104981200-104982200 Enhancers Fetal Intestine Large intestine
7 chr11:104981200-104983000 Enhancers Hela-S3 cervix
8 chr11:104981400-104982000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr11:104981600-104982000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
10 chr11:104981600-104982200 Enhancers Placenta Placenta
11 chr11:104981600-104982200 Enhancers HUVEC blood vessel

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