| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:45083984-45084202 | Common:1; Rare:73 | ||||
| chr14:45135644-45136023 | Common:1; Rare:87 | ||||
| chr14:49586342-49586720 | Common:1; Rare:197 | ||||
| chr14:49598665-49598996 | Common:1; Rare:127 | ||||
| chr14:49620431-49620830 | Common:3; Rare:139; Clinvar:3 | ||||
| chr14:49621252-49621379 | Rare:49; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49688201-49688316 | Rare:40 | ||||
| chr14:49692932-49693185 | Common:1; Rare:83 | ||||
| chr14:49767482-49767706 | Common:2; Rare:84 | ||||
| chr14:49767998-49768337 | Common:2; Rare:115 | ||||
| chr14:49768817-49768988 | Rare:39 | ||||
| chr14:49852718-49852926 | Common:2; Rare:75 | ||||
| chr14:49852998-49853149 | Rare:30 | ||||
| chr14:49892898-49893142 | Rare:104 | ||||
| chr14:50116551-50116696 | Rare:67 |