Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73058424-73058583 | Common:2; Rare:54 | ||||
chr14:73536994-73537194 | Common:3; Rare:22 | ||||
chr14:73569178-73569292 | Rare:37 | ||||
chr14:73644871-73645037 | Common:3; Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
chr14:73787175-73787353 | Common:2; Rare:70 | ||||
chr14:73851741-73851976 | Common:4; Rare:81 | ||||
chr14:73950080-73950323 | Common:5; Rare:96; Clinvar (benign):3 | ||||
chr14:74019248-74019436 | Common:1; Rare:74 | ||||
chr14:74493219-74493781 | Common:4; Rare:181; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:74713058-74713213 | Rare:84 | ||||
chr14:74881733-74881968 | Common:1; Rare:100 | ||||
chr14:75002741-75002982 | Common:1; Rare:79; Clinvar:2 | ||||
chr14:75127001-75127110 | Rare:33 | ||||
chr14:75660797-75661327 | Common:4; Rare:127 | ||||
chr14:77320847-77321105 | Rare:81; Clinvar:1 |