| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56729949-56730189 | Common:1; Rare:58 | ||||
| chr16:56781774-56781859 | Rare:12 | ||||
| chr16:56931939-56932214 | Common:2; Rare:145 | ||||
| chr16:57185891-57186339 | Common:2; Rare:126 | ||||
| chr16:57447360-57447508 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:57639267-57639535 | Rare:58; Clinvar (pathogenic):1 | ||||
| chr16:58001340-58001440 | Rare:31 | ||||
| chr16:58129238-58129572 | Common:3; Rare:102 | ||||
| chr16:58249840-58250006 | Rare:44 | ||||
| chr16:58684704-58684853 | Common:1; Rare:42 | ||||
| chr16:62036269-62036597 | Rare:74 | ||||
| chr16:65122005-65122202 | Common:1; Rare:66 | ||||
| chr16:66552512-66552649 | Rare:60 | ||||
| chr16:66751591-66751886 | Common:3; Rare:82 | ||||
| chr16:66934327-66934506 | Common:1; Rare:73 |