| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74019237-74019455 | Common:1; Rare:79 | ||||
| chr14:74493371-74493797 | Common:4; Rare:134; Clinvar (benign):4 | ||||
| chr14:74713042-74713203 | Rare:91 | ||||
| chr14:74763160-74763425 | Rare:84 | ||||
| chr14:75002741-75002968 | Common:1; Rare:68; Clinvar:2 | ||||
| chr14:75126985-75127104 | Rare:39 | ||||
| chr14:75279079-75279362 | Common:1; Rare:66 | ||||
| chr14:75427653-75427745 | Rare:21 | ||||
| chr14:75660789-75661055 | Rare:71 | ||||
| chr14:75661173-75661330 | Common:2; Rare:43 | ||||
| chr14:76151757-76151982 | Rare:82 | ||||
| chr14:76152410-76152510 | Common:3; Rare:20 | ||||
| chr14:77320867-77321099 | Rare:71; Clinvar:1 | ||||
| chr14:77377022-77377415 | Common:3; Rare:117 | ||||
| chr14:77457550-77457878 | Common:1; Rare:97 |