Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:74019263-74019429 | Common:1; Rare:64 | ||||
chr14:74493249-74493781 | Common:4; Rare:169; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:74713053-74713205 | Rare:84 | ||||
chr14:74763070-74763408 | Rare:96 | ||||
chr14:75002666-75002982 | Common:1; Rare:105; Clinvar:2 | ||||
chr14:75126994-75127106 | Rare:34 | ||||
chr14:75279474-75279660 | Rare:39 | ||||
chr14:75522190-75522458 | Rare:49 | ||||
chr14:75660800-75661326 | Common:4; Rare:125 | ||||
chr14:77320838-77321051 | Rare:64; Clinvar:1 | ||||
chr14:77376969-77377410 | Common:5; Rare:127 | ||||
chr14:77457561-77457844 | Common:1; Rare:88 | ||||
chr14:77708000-77708133 | Common:1; Rare:68 | ||||
chr14:77761114-77761252 | Rare:54 | ||||
chr14:81220871-81221054 | Common:1; Rare:87 |