| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103715409-103715831 | Common:1; Rare:141 | ||||
| chr14:103921473-103921736 | Common:3; Rare:79 | ||||
| chr14:104924733-104924944 | Common:1; Rare:41 | ||||
| chr14:105248419-105248587 | Common:4; Rare:71 | ||||
| chr14:105419737-105420033 | Rare:94 | ||||
| chr15:22838433-22838762 | Common:3; Rare:130 | ||||
| chr15:23039469-23039698 | Common:1; Rare:105 | ||||
| chr15:25438972-25439278 | Common:3; Rare:121 | ||||
| chr15:34101849-34102123 | Common:1; Rare:54 | ||||
| chr15:34209992-34210113 | Common:1; Rare:52 | ||||
| chr15:34224952-34225146 | Rare:74 | ||||
| chr15:34343068-34343180 | Common:2; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:34367150-34367285 | Rare:50 | ||||
| chr15:34582754-34582894 | Rare:41 | ||||
| chr15:34588443-34588542 | Rare:31 |