Variant report

Variant rs12431783
Chromosome Location chr14:32188884-32188885
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32171000-32200600 Weak transcription Placenta Amnion Placenta Amnion
2 chr14:32173400-32189800 Weak transcription Primary B cells from cord blood blood
3 chr14:32173400-32218000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr14:32174600-32200000 Weak transcription Primary T helper naive cells fromperipheralblood blood
5 chr14:32175400-32193400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr14:32175400-32205600 Weak transcription Ovary ovary
7 chr14:32181400-32200600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr14:32186800-32205600 Weak transcription Primary T cells from cord blood blood
9 chr14:32187200-32196000 Weak transcription Aorta Aorta
10 chr14:32187400-32199000 Weak transcription HepG2 liver
11 chr14:32188600-32189600 Weak transcription Fetal Heart heart

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