| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103467841-103468011 | Common:2; Rare:35 | ||||
| chr14:103529032-103529266 | Common:1; Rare:71 | ||||
| chr14:103562593-103563238 | Common:11; Rare:264; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103629133-103629490 | Common:4; Rare:133 | ||||
| chr14:103715412-103715924 | Common:1; Rare:170 | ||||
| chr14:104753116-104753311 | Common:1; Rare:85 | ||||
| chr14:104773912-104774186 | Common:1; Rare:81; Clinvar (benign):3 | ||||
| chr14:104970451-104970554 | Common:2; Rare:16 | ||||
| chr14:104985626-104985853 | Common:3; Rare:91 | ||||
| chr14:105021031-105021386 | Common:1; Rare:127 | ||||
| chr14:105248421-105248608 | Common:6; Rare:90 | ||||
| chr14:105300909-105301117 | Rare:58 | ||||
| chr14:105419723-105420032 | Rare:99 | ||||
| chr15:22838467-22838768 | Common:3; Rare:117 | ||||
| chr15:22980292-22980508 | Rare:81 |