| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105490991-105491424 | Common:1; Rare:132 | ||||
| chr14:105491581-105491767 | Common:1; Rare:81 | ||||
| chr14:105526489-105526662 | Common:1; Rare:35 | ||||
| chr14:105528448-105528623 | Rare:39 | ||||
| chr15:22786138-22786291 | Rare:37 | ||||
| chr15:22786319-22786832 | Common:2; Rare:166; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:22838055-22838269 | Common:3; Rare:47 | ||||
| chr15:22838357-22839111 | Common:7; Rare:237 | ||||
| chr15:22980167-22980479 | Common:3; Rare:122 | ||||
| chr15:23038823-23039234 | Common:6; Rare:115 | ||||
| chr15:23039313-23039335 | Rare:8 | ||||
| chr15:23039472-23039846 | Common:1; Rare:154 | ||||
| chr15:24954939-24955065 | Rare:71 | ||||
| chr15:25438168-25438466 | Common:1; Rare:93 | ||||
| chr15:25438681-25438852 | Rare:50 |