Variant report

Variant rs66846966
Chromosome Location chr9:21752922-21752923
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:21748400-21754400 Weak transcription Hela-S3 cervix
2 chr9:21748600-21754400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr9:21748800-21754400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr9:21751000-21754000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr9:21751200-21753600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr9:21751200-21753600 Weak transcription NHEK skin
7 chr9:21751200-21754000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr9:21752200-21753600 Weak transcription HMEC breast
9 chr9:21752800-21753000 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell

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