| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31026835-31027039 | Common:2; Rare:46 | ||||
| chr14:31205960-31206240 | Rare:49 | ||||
| chr14:31206722-31206945 | Rare:50 | ||||
| chr14:31206964-31207109 | Common:2; Rare:32 | ||||
| chr14:31207220-31207330 | Rare:29 | ||||
| chr14:31207440-31207744 | Common:2; Rare:99 | ||||
| chr14:31207751-31208026 | Rare:86 | ||||
| chr14:31208039-31208236 | Common:2; Rare:58 | ||||
| chr14:31208243-31208416 | Rare:36 | ||||
| chr14:31420452-31420773 | Common:6; Rare:102 | ||||
| chr14:31420991-31421040 | Common:1; Rare:8 | ||||
| chr14:31456964-31457056 | Rare:16 | ||||
| chr14:31457264-31457617 | Common:3; Rare:116 | ||||
| chr14:31561087-31561523 | Common:4; Rare:125; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:32076245-32076326 | Rare:24 |