| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103333690-103334323 | Common:6; Rare:233 | ||||
| chr14:103334610-103334847 | Common:1; Rare:109 | ||||
| chr14:103335058-103335081 | Rare:7 | ||||
| chr14:103335109-103335153 | Rare:12 | ||||
| chr14:103335441-103335633 | Common:1; Rare:51 | ||||
| chr14:103385143-103385623 | Common:1; Rare:156 | ||||
| chr14:103386134-103386190 | Rare:16 | ||||
| chr14:103386233-103386315 | Common:2; Rare:20 | ||||
| chr14:103521089-103521285 | Common:1; Rare:68 | ||||
| chr14:103529061-103529268 | Common:1; Rare:60 | ||||
| chr14:103561832-103562063 | Common:4; Rare:90 | ||||
| chr14:103562546-103563297 | Common:11; Rare:312; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103628714-103628741 | Rare:10 | ||||
| chr14:103628814-103629502 | Common:8; Rare:210 | ||||
| chr14:103715372-103715920 | Common:1; Rare:186 |