| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58630347-58630611 | Common:1; Rare:66 | ||||
| chr16:58684686-58684820 | Rare:38 | ||||
| chr16:58734236-58734424 | Common:4; Rare:58 | ||||
| chr16:62034790-62035212 | Common:6; Rare:118 | ||||
| chr16:62035210-62035320 | Common:3; Rare:39 | ||||
| chr16:62036360-62036660 | Rare:76 | ||||
| chr16:65059470-65059593 | Common:1; Rare:30 | ||||
| chr16:65122044-65122406 | Common:1; Rare:100 | ||||
| chr16:66516833-66517233 | Rare:101; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr16:66549817-66549982 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:66550064-66550211 | Common:2; Rare:75; Clinvar (benign):2 | ||||
| chr16:66552434-66552588 | Rare:71 | ||||
| chr16:66604453-66604746 | Rare:79 | ||||
| chr16:66605415-66605913 | Common:5; Rare:197 | ||||
| chr16:66696686-66696950 | Common:5; Rare:103 |