| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:104752826-104753286 | Common:8; Rare:383 | ||||
| chr14:104753893-104754663 | Common:7; Rare:332 | ||||
| chr14:104774349-104774749 | Common:5; Rare:124 | ||||
| chr14:104775686-104776955 | Common:31; Rare:564; Clinvar:8; Clinvar (benign):5 | ||||
| chr14:104794061-104794461 | Common:4; Rare:204 | ||||
| chr14:104794628-104794826 | Common:2; Rare:60 | ||||
| chr14:104794834-104795247 | Common:2; Rare:144 | ||||
| chr14:104795514-104795938 | Rare:233 | ||||
| chr14:104800387-104800814 | Common:10; Rare:288 | ||||
| chr14:104800841-104801212 | Common:2; Rare:216 | ||||
| chr14:104864512-104865463 | Common:22; Rare:433 | ||||
| chr14:104865640-104866190 | Common:1; Rare:127 | ||||
| chr14:104970434-104970801 | Common:8; Rare:133 | ||||
| chr14:104978326-104978626 | Common:2; Rare:158 | ||||
| chr14:104985591-104986049 | Common:12; Rare:343 |