Variant report

Variant rs4981891
Chromosome Location chr14:32193959-32193960
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 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 chr14:32175400-32205600 Weak transcription Ovary ovary
5 chr14:32181400-32200600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr14:32186800-32205600 Weak transcription Primary T cells from cord blood blood
7 chr14:32187200-32196000 Weak transcription Aorta Aorta
8 chr14:32187400-32199000 Weak transcription HepG2 liver

Quick Search:


  
Input of quick search could be:

what's new

Quick links