| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:59361390-59362020 | Common:3; Rare:107 | ||||
| chr14:59465038-59465730 | Common:15; Rare:298 | ||||
| chr14:59483863-59485342 | Common:27; Rare:904 | ||||
| chr14:59630598-59630804 | Rare:61 | ||||
| chr14:59870701-59870957 | Common:2; Rare:60 | ||||
| chr14:60091707-60092363 | Common:21; Rare:519 | ||||
| chr14:60092360-60092968 | Common:6; Rare:174 | ||||
| chr14:60164722-60164940 | Common:2; Rare:52 | ||||
| chr14:60165111-60165436 | Rare:124 | ||||
| chr14:60248810-60249484 | Common:15; Rare:493 | ||||
| chr14:60249654-60250010 | Common:6; Rare:265 | ||||
| chr14:60514940-60515290 | Common:2; Rare:95 | ||||
| chr14:60649383-60649750 | Common:8; Rare:229; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:60652980-60653470 | Common:2; Rare:86 | ||||
| chr14:60657560-60658270 | Common:1; Rare:192 |