| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30876485-30876734 | Common:1; Rare:46 | ||||
| chr16:30902211-30902382 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:30902481-30902619 | Rare:50; Clinvar:6 | ||||
| chr16:30903699-30903915 | Common:1; Rare:29 | ||||
| chr16:30921691-30921923 | Common:1; Rare:39 | ||||
| chr16:30949992-30950377 | Rare:73 | ||||
| chr16:30958300-30958413 | Rare:25 | ||||
| chr16:31107626-31107739 | Rare:19 | ||||
| chr16:31113938-31114088 | Rare:19 | ||||
| chr16:31178992-31179141 | Rare:17 | ||||
| chr16:31201625-31201880 | Rare:96 | ||||
| chr16:31265440-31265654 | Common:3; Rare:49 | ||||
| chr16:31266055-31266124 | Rare:15 | ||||
| chr16:31352542-31352586 | Rare:8 | ||||
| chr16:31386683-31386942 | Rare:42 |