| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73027058-73027367 | Common:2; Rare:83 | ||||
| chr14:73058301-73058637 | Common:3; Rare:103 | ||||
| chr14:73136361-73136550 | Common:4; Rare:67; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:73458513-73458901 | Common:6; Rare:104 | ||||
| chr14:73569061-73569292 | Rare:57 | ||||
| chr14:73644834-73645049 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73787121-73787394 | Common:2; Rare:91 | ||||
| chr14:73851733-73851983 | Common:4; Rare:85 | ||||
| chr14:73950027-73950334 | Common:6; Rare:128; Clinvar (benign):5 | ||||
| chr14:74019237-74019436 | Common:1; Rare:77 | ||||
| chr14:74302915-74303095 | Common:1; Rare:72; Clinvar (benign):1 | ||||
| chr14:74493385-74493832 | Common:4; Rare:149; Clinvar (benign):4 | ||||
| chr14:74713042-74713213 | Rare:96 | ||||
| chr14:74763150-74763420 | Rare:86 | ||||
| chr14:74763564-74763652 | Rare:32 |