| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100376754-100376958 | Rare:30 | ||||
| chr14:101809736-101809912 | Rare:36 | ||||
| chr14:101964238-101964634 | Common:4; Rare:109; Clinvar:1 | ||||
| chr14:102139662-102139935 | Rare:97 | ||||
| chr14:102305131-102305284 | Common:1; Rare:54 | ||||
| chr14:102362858-102363092 | Rare:105 | ||||
| chr14:103333969-103334252 | Common:1; Rare:117 | ||||
| chr14:103529091-103529243 | Common:1; Rare:48 | ||||
| chr14:103562620-103563280 | Common:11; Rare:271; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103673158-103673366 | Common:1; Rare:49 | ||||
| chr14:103715489-103715860 | Common:1; Rare:120 | ||||
| chr14:104970469-104970776 | Common:4; Rare:63 | ||||
| chr14:105477149-105477271 | Common:1; Rare:24 | ||||
| chr15:22838356-22838748 | Common:3; Rare:140 | ||||
| chr15:22980292-22980497 | Rare:74 |