| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74763470-74763930 | Rare:145 | ||||
| chr14:74881676-74882076 | Common:3; Rare:419 | ||||
| chr14:74882239-74882761 | Common:7; Rare:205 | ||||
| chr14:74922821-74923530 | Common:11; Rare:273 | ||||
| chr14:74955471-74955871 | Common:3; Rare:129 | ||||
| chr14:75002470-75003110 | Common:6; Rare:680; Clinvar:12; Clinvar (pathogenic):2 | ||||
| chr14:75051314-75051714 | Common:9; Rare:212; Clinvar:11; Clinvar (benign):7 | ||||
| chr14:75063530-75063790 | Common:1; Rare:55 | ||||
| chr14:75063797-75064199 | Common:5; Rare:344 | ||||
| chr14:75068804-75069204 | Common:10; Rare:130 | ||||
| chr14:75069175-75069763 | Common:15; Rare:805 | ||||
| chr14:75070400-75070790 | Common:8; Rare:178 | ||||
| chr14:75126044-75126444 | Rare:88 | ||||
| chr14:75126660-75126920 | Common:2; Rare:69 | ||||
| chr14:75126940-75127570 | Common:10; Rare:549 |