| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:90266693-90266834 | Common:1; Rare:28 | ||||
| chr14:90383193-90383512 | Common:3; Rare:108 | ||||
| chr14:90828153-90828392 | Common:2; Rare:62 | ||||
| chr14:91222587-91222802 | Common:1; Rare:45 | ||||
| chr14:91241791-91241894 | Common:1; Rare:12 | ||||
| chr14:91241986-91242149 | Common:1; Rare:26 | ||||
| chr14:91462757-91463045 | Common:1; Rare:58 | ||||
| chr14:91873524-91873658 | Common:1; Rare:23 | ||||
| chr14:92459388-92459705 | Common:1; Rare:70 | ||||
| chr14:92633337-92633443 | Rare:17 | ||||
| chr14:92669771-92670037 | Common:3; Rare:30 | ||||
| chr14:92713821-92714136 | Common:1; Rare:61 | ||||
| chr14:94380984-94381335 | Common:4; Rare:107; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:94387645-94387703 | Rare:11 | ||||
| chr14:94387738-94387859 | Rare:17 |