| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103562624-103563222 | Common:11; Rare:249; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103921480-103921676 | Common:3; Rare:66 | ||||
| chr14:104604752-104604862 | Common:6; Rare:48 | ||||
| chr14:104752995-104753208 | Common:2; Rare:79 | ||||
| chr14:105021053-105021376 | Common:1; Rare:114 | ||||
| chr14:105419733-105420032 | Rare:95 | ||||
| chr15:23039546-23039651 | Common:1; Rare:44 | ||||
| chr15:23565511-23565685 | Common:1; Rare:46 | ||||
| chr15:25439006-25439245 | Common:2; Rare:90 | ||||
| chr15:30903694-30903936 | Common:1; Rare:62 | ||||
| chr15:31870625-31870943 | Rare:102 | ||||
| chr15:32615117-32615571 | Common:6; Rare:116 | ||||
| chr15:32641608-32641766 | Common:2; Rare:40 | ||||
| chr15:34101840-34102083 | Common:1; Rare:50 | ||||
| chr15:34583638-34583757 | Common:2; Rare:39 |