| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103333951-103334246 | Common:2; Rare:120 | ||||
| chr14:103334628-103334812 | Common:1; Rare:82 | ||||
| chr14:103529049-103529243 | Common:1; Rare:58 | ||||
| chr14:103562620-103563112 | Common:8; Rare:198; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:103629074-103629491 | Common:4; Rare:161 | ||||
| chr14:103715437-103715853 | Common:1; Rare:140 | ||||
| chr14:103921475-103921676 | Common:3; Rare:67 | ||||
| chr14:104604748-104604879 | Common:6; Rare:54 | ||||
| chr14:104752973-104753208 | Common:2; Rare:86 | ||||
| chr14:104985672-104985795 | Common:2; Rare:42 | ||||
| chr14:105021041-105021386 | Common:1; Rare:122 | ||||
| chr14:105315519-105315536 | Rare:4 | ||||
| chr14:105419728-105420037 | Rare:99 | ||||
| chr14:105474497-105474889 | Common:1; Rare:116 | ||||
| chr14:105487053-105487226 | Common:1; Rare:53 |