| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:30558987-30559264 | Common:8; Rare:246 | ||||
| chr14:30622127-30622449 | Common:2; Rare:284 | ||||
| chr14:30874313-30874606 | Common:3; Rare:179 | ||||
| chr14:31025386-31025786 | Common:6; Rare:185; Clinvar (benign):1 | ||||
| chr14:31025976-31026781 | Common:16; Rare:478 | ||||
| chr14:31026821-31027178 | Common:4; Rare:120 | ||||
| chr14:31205795-31206286 | Rare:176 | ||||
| chr14:31207390-31208332 | Common:12; Rare:722 | ||||
| chr14:31419250-31420210 | Common:7; Rare:372 | ||||
| chr14:31420382-31420791 | Common:14; Rare:308 | ||||
| chr14:31457350-31457653 | Common:4; Rare:160 | ||||
| chr14:31561314-31561533 | Common:4; Rare:153; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr14:32076407-32077395 | Common:11; Rare:599 | ||||
| chr14:32077897-32079074 | Common:7; Rare:370 | ||||
| chr14:32939698-32939997 | Rare:101 |