| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:102139651-102139932 | Rare:99 | ||||
| chr14:102305048-102305305 | Common:1; Rare:79 | ||||
| chr14:102362862-102363093 | Rare:103 | ||||
| chr14:103333967-103334246 | Common:1; Rare:114 | ||||
| chr14:103529134-103529243 | Common:1; Rare:43 | ||||
| chr14:103562624-103563085 | Common:8; Rare:182; Clinvar (benign):5 | ||||
| chr14:103629133-103629484 | Common:4; Rare:129 | ||||
| chr14:105021024-105021387 | Common:1; Rare:130 | ||||
| chr14:105419733-105420032 | Rare:95 | ||||
| chr15:23039544-23039698 | Common:1; Rare:60 | ||||
| chr15:23565509-23565697 | Common:2; Rare:53 | ||||
| chr15:23566200-23566338 | Rare:74; Clinvar (pathogenic):1 | ||||
| chr15:23647801-23647946 | Rare:40 | ||||
| chr15:24823589-24823716 | Common:1; Rare:32; Clinvar:1 | ||||
| chr15:26866976-26867096 | Common:3; Rare:33 |