| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103521465-103521805 | Common:2; Rare:96 | ||||
| chr14:103522817-103523015 | Rare:61 | ||||
| chr14:103529049-103529243 | Common:1; Rare:58 | ||||
| chr14:103562624-103563044 | Common:8; Rare:164; Clinvar (benign):5 | ||||
| chr14:103629110-103629403 | Common:2; Rare:115 | ||||
| chr14:103715435-103715860 | Common:1; Rare:144 | ||||
| chr14:104773249-104773493 | Rare:58; Clinvar:4; Clinvar (benign):6 | ||||
| chr14:104800928-104801066 | Rare:37 | ||||
| chr14:104985646-104985800 | Common:3; Rare:57 | ||||
| chr14:105301009-105301117 | Rare:19 | ||||
| chr14:105419733-105420032 | Rare:95 | ||||
| chr15:25438984-25439173 | Common:2; Rare:70 | ||||
| chr15:29269779-29270055 | Common:1; Rare:94 | ||||
| chr15:30903779-30903954 | Rare:44 | ||||
| chr15:31870638-31870935 | Rare:93 |