| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103562623-103563104 | Common:8; Rare:193; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:103715502-103715853 | Common:1; Rare:112 | ||||
| chr14:105021018-105021376 | Common:1; Rare:131 | ||||
| chr14:105419737-105420018 | Rare:84 | ||||
| chr14:105487109-105487236 | Common:1; Rare:43 | ||||
| chr15:23039519-23039730 | Common:1; Rare:92 | ||||
| chr15:23687248-23687415 | Common:1; Rare:59 | ||||
| chr15:25438986-25439261 | Common:2; Rare:112 | ||||
| chr15:26629068-26629142 | Rare:20 | ||||
| chr15:29269791-29269865 | Rare:28 | ||||
| chr15:30903666-30903943 | Common:2; Rare:74 | ||||
| chr15:30991591-30991947 | Common:5; Rare:123 | ||||
| chr15:32615127-32615613 | Common:7; Rare:119 | ||||
| chr15:34101821-34102083 | Common:1; Rare:59 | ||||
| chr15:34224881-34225126 | Rare:87 |