Variant report

Variant rs74088524
Chromosome Location chr14:104812623-104812624
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104809200-104815200 Weak transcription Gastric stomach
2 chr14:104810400-104815400 Weak transcription Brain Germinal Matrix brain
3 chr14:104812200-104812800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr14:104812200-104812800 Enhancers Placenta Amnion Placenta Amnion
5 chr14:104812400-104812800 Enhancers Placenta Placenta
6 chr14:104812400-104813200 Enhancers Hela-S3 cervix
7 chr14:104812400-104813400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr14:104812600-104812800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr14:104812600-104812800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr14:104812600-104812800 Enhancers Esophagus oesophagus
11 chr14:104812600-104812800 Bivalent Enhancer NHEK skin

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