| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:58267288-58267543 | Rare:54 | ||||
| chr14:61568738-61568902 | Common:2; Rare:45 | ||||
| chr14:61569886-61570141 | Common:2; Rare:44 | ||||
| chr14:61570609-61570672 | Rare:12 | ||||
| chr14:61751065-61751232 | Rare:45 | ||||
| chr14:63990907-63990971 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chr14:64186283-64186553 | Common:1; Rare:81; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:64211877-64212006 | Rare:27 | ||||
| chr14:64224327-64224502 | Common:3; Rare:56; Clinvar:3; Clinvar (benign):4 | ||||
| chr14:65301955-65302254 | Common:1; Rare:44 | ||||
| chr14:65318722-65319092 | Common:2; Rare:59 | ||||
| chr14:65468382-65468553 | Common:4; Rare:33 | ||||
| chr14:68384839-68385136 | Rare:45 | ||||
| chr14:68685424-68685729 | Common:1; Rare:54 | ||||
| chr14:68780163-68780262 | Rare:22 |