| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103562615-103563048 | Common:8; Rare:169; Clinvar (benign):5 | ||||
| chr14:103715442-103715883 | Common:1; Rare:146 | ||||
| chr14:104104800-104104988 | Rare:40 | ||||
| chr14:104111432-104111472 | Rare:13 | ||||
| chr14:104776738-104776848 | Rare:30; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:104970432-104970833 | Common:4; Rare:75 | ||||
| chr14:105487098-105487270 | Common:2; Rare:63 | ||||
| chr15:23039539-23039650 | Common:1; Rare:47 | ||||
| chr15:25438963-25439182 | Common:3; Rare:79 | ||||
| chr15:28099277-28099538 | Common:2; Rare:94; Clinvar:1 | ||||
| chr15:29269798-29269924 | Common:1; Rare:49 | ||||
| chr15:30903668-30903974 | Common:2; Rare:84 | ||||
| chr15:31326535-31326847 | Rare:129 | ||||
| chr15:31365869-31366141 | Common:3; Rare:74 | ||||
| chr15:32615111-32615589 | Common:6; Rare:121 |