Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:69398253-69398430 | Common:1; Rare:68 | ||||
chr14:72926196-72926524 | Common:6; Rare:79 | ||||
chr14:73058301-73058574 | Common:2; Rare:80 | ||||
chr14:73644901-73645030 | Common:2; Rare:36; Clinvar:2 | ||||
chr14:73851723-73851974 | Common:4; Rare:82 | ||||
chr14:73886765-73886869 | Common:1; Rare:33 | ||||
chr14:73950175-73950322 | Common:3; Rare:62; Clinvar (benign):1 | ||||
chr14:74493569-74493777 | Common:3; Rare:78; Clinvar (benign):4 | ||||
chr14:74713053-74713210 | Rare:86 | ||||
chr14:75660781-75660939 | Rare:45 | ||||
chr14:75661183-75661299 | Common:2; Rare:30 | ||||
chr14:77098014-77098258 | Rare:66 | ||||
chr14:77377082-77377403 | Common:1; Rare:83 | ||||
chr14:77457561-77457876 | Common:1; Rare:93 | ||||
chr14:77708011-77708164 | Common:2; Rare:83 |