| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48709369-48709667 | Common:4; Rare:45 | ||||
| chr13:48710166-48710325 | Rare:24 | ||||
| chr14:22771289-22771441 | Rare:69 | ||||
| chr14:34874061-34874210 | Common:1; Rare:39 | ||||
| chr14:49633960-49634076 | Common:1; Rare:47; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:73099429-73099742 | Common:2; Rare:44 | ||||
| chr14:73245985-73246107 | Common:2; Rare:52 | ||||
| chr15:29268701-29269013 | Common:3; Rare:103; Clinvar (pathogenic):1 | ||||
| chr15:31061588-31061743 | Rare:26 | ||||
| chr15:40032059-40032238 | Common:1; Rare:36 | ||||
| chr15:52417527-52417760 | Common:3; Rare:46 | ||||
| chr15:74954492-74954625 | Rare:24 | ||||
| chr15:81003330-81003508 | Rare:64 | ||||
| chr15:81003651-81003690 | Common:1; Rare:7 | ||||
| chr15:82750460-82750599 | Common:2; Rare:37 |