| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100376264-100376495 | Common:3; Rare:77 | ||||
| chr14:101809718-101809912 | Rare:42 | ||||
| chr14:101964377-101964647 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:102086989-102087377 | Common:5; Rare:164 | ||||
| chr14:102139654-102139920 | Rare:92 | ||||
| chr14:102362855-102363092 | Rare:105 | ||||
| chr14:103333917-103334252 | Common:3; Rare:142 | ||||
| chr14:103529084-103529235 | Common:1; Rare:47 | ||||
| chr14:103562620-103563044 | Common:8; Rare:165; Clinvar (benign):5 | ||||
| chr14:103715437-103715842 | Common:1; Rare:132 | ||||
| chr14:105021031-105021376 | Common:1; Rare:124 | ||||
| chr14:105176974-105177378 | Common:3; Rare:111 | ||||
| chr14:105419733-105420027 | Rare:89 | ||||
| chr15:22838356-22838762 | Common:3; Rare:146 | ||||
| chr15:23039541-23039698 | Common:1; Rare:63 |