| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103333924-103334242 | Common:3; Rare:135 | ||||
| chr14:103529058-103529235 | Common:1; Rare:51 | ||||
| chr14:103562623-103563059 | Common:8; Rare:173; Clinvar (benign):5 | ||||
| chr14:103715437-103715853 | Common:1; Rare:140 | ||||
| chr14:104985646-104985810 | Common:3; Rare:63 | ||||
| chr14:105021044-105021373 | Common:1; Rare:115 | ||||
| chr14:105419733-105420032 | Rare:95 | ||||
| chr15:23039529-23039707 | Common:1; Rare:75 | ||||
| chr15:23687237-23687435 | Common:1; Rare:75 | ||||
| chr15:25438984-25439237 | Common:2; Rare:97 | ||||
| chr15:28099293-28099525 | Common:2; Rare:82; Clinvar:1 | ||||
| chr15:29269798-29269880 | Rare:30 | ||||
| chr15:30903792-30903946 | Rare:36 | ||||
| chr15:32615099-32615603 | Common:7; Rare:127 | ||||
| chr15:33194694-33194943 | Common:1; Rare:68 |