Variant report

Variant rs66472756
Chromosome Location chr14:32191132-32191133
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32171000-32200600 Weak transcription Placenta Amnion Placenta Amnion
2 chr14:32173400-32218000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr14:32174600-32200000 Weak transcription Primary T helper naive cells fromperipheralblood blood
4 chr14:32175400-32193400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr14:32175400-32205600 Weak transcription Ovary ovary
6 chr14:32181400-32200600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr14:32186800-32205600 Weak transcription Primary T cells from cord blood blood
8 chr14:32187200-32196000 Weak transcription Aorta Aorta
9 chr14:32187400-32199000 Weak transcription HepG2 liver

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