| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103489210-103489343 | Rare:17 | ||||
| chr14:103529107-103529258 | Common:1; Rare:52 | ||||
| chr14:103562586-103563048 | Common:8; Rare:180; Clinvar (benign):5 | ||||
| chr14:103629373-103629496 | Common:2; Rare:42 | ||||
| chr14:103715435-103715913 | Common:1; Rare:158 | ||||
| chr14:104752994-104753283 | Common:2; Rare:110 | ||||
| chr14:104753942-104753967 | Common:1; Rare:5 | ||||
| chr14:104985626-104985840 | Common:3; Rare:87 | ||||
| chr14:105021079-105021379 | Common:1; Rare:106 | ||||
| chr14:105248426-105248625 | Common:6; Rare:98 | ||||
| chr14:105300996-105301116 | Rare:26 | ||||
| chr14:105419723-105420059 | Rare:102 | ||||
| chr14:105449119-105449407 | Rare:75 | ||||
| chr14:105487061-105487197 | Common:1; Rare:35 | ||||
| chr15:22838433-22839068 | Common:5; Rare:210 |