Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:67412109-67412334 | Common:1; Rare:51 | ||||
chr14:67816578-67816732 | Rare:27 | ||||
chr14:68979181-68979559 | Common:2; Rare:113 | ||||
chr14:69191434-69191548 | Rare:22 | ||||
chr14:69398238-69398425 | Common:1; Rare:75 | ||||
chr14:69398586-69398710 | Rare:30 | ||||
chr14:69611480-69611708 | Common:1; Rare:78 | ||||
chr14:70416971-70417140 | Rare:53 | ||||
chr14:71320258-71320491 | Rare:73 | ||||
chr14:73058309-73058587 | Common:3; Rare:83 | ||||
chr14:73787175-73787350 | Common:2; Rare:70 | ||||
chr14:73851750-73851976 | Common:4; Rare:78 | ||||
chr14:73886780-73886893 | Common:2; Rare:37 | ||||
chr14:73950106-73950323 | Common:5; Rare:83; Clinvar (benign):3 | ||||
chr14:74019254-74019428 | Common:1; Rare:68 |