Variant report

Variant rs61485460
Chromosome Location chr12:104595038-104595039
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:104594000-104595200 Weak transcription H1 Cell Line embryonic stem cell
2 chr12:104594800-104595200 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood
3 chr12:104594800-104595400 Enhancers Brain Cingulate Gyrus brain
4 chr12:104594800-104595400 Enhancers NHLF lung
5 chr12:104595000-104595200 Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
6 chr12:104595000-104595400 Enhancers Colon Smooth Muscle Colon
7 chr12:104595000-104595600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr12:104595000-104595600 Enhancers A549 lung
9 chr12:104595000-104595600 Enhancers Osteobl bone

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