| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19067455-19067611 | Common:4; Rare:42 | ||||
| chr16:20806419-20806530 | Rare:46 | ||||
| chr16:22297217-22297440 | Common:2; Rare:102 | ||||
| chr16:22436949-22437037 | Rare:33 | ||||
| chr16:23557336-23557425 | Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641246-23641525 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678710-23678939 | Common:4; Rare:72 | ||||
| chr16:24729604-24729727 | Common:6; Rare:68 | ||||
| chr16:25111490-25111782 | Common:2; Rare:77 | ||||
| chr16:27268717-27268850 | Common:1; Rare:43 | ||||
| chr16:27313796-27313954 | Common:1; Rare:45 | ||||
| chr16:27549891-27550161 | Common:2; Rare:95 | ||||
| chr16:28822695-28822732 | Rare:15 | ||||
| chr16:28925173-28925405 | Rare:76 | ||||
| chr16:29973611-29973938 | Common:5; Rare:111 |