| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:34874791-34874929 | Common:1; Rare:37 | ||||
| chr14:34874874-34875025 | Common:1; Rare:53 | ||||
| chr14:34875145-34875456 | Rare:180 | ||||
| chr14:34982438-34982732 | Common:2; Rare:221 | ||||
| chr14:35046088-35046539 | Common:4; Rare:294 | ||||
| chr14:35046830-35047260 | Common:8; Rare:150 | ||||
| chr14:35121660-35121930 | Rare:137 | ||||
| chr14:35122200-35122805 | Common:4; Rare:286 | ||||
| chr14:35292174-35292486 | Common:10; Rare:222; Clinvar:2 | ||||
| chr14:35402730-35403210 | Common:7; Rare:245; Clinvar (benign):5 | ||||
| chr14:35403213-35403540 | Rare:163; Clinvar:7 | ||||
| chr14:35403662-35404222 | Common:3; Rare:310; Clinvar:2; Clinvar (benign):5 | ||||
| chr14:35404576-35404913 | Common:4; Rare:194; Clinvar:1; Clinvar (benign):4 | ||||
| chr14:35826071-35826490 | Common:2; Rare:206 | ||||
| chr14:35826702-35826938 | Common:1; Rare:65 |