| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30527280-30527566 | Common:1; Rare:78 | ||||
| chr16:30534575-30534633 | Rare:21 | ||||
| chr16:30534834-30535089 | Common:3; Rare:83 | ||||
| chr16:30571550-30571786 | Rare:74 | ||||
| chr16:30585532-30585937 | Common:1; Rare:92 | ||||
| chr16:30650462-30651010 | Rare:137 | ||||
| chr16:30658649-30658883 | Common:1; Rare:70 | ||||
| chr16:30697969-30698282 | Common:1; Rare:141 | ||||
| chr16:30698325-30698454 | Rare:51 | ||||
| chr16:30698506-30698732 | Common:1; Rare:76 | ||||
| chr16:30698991-30699394 | Rare:108; Clinvar (benign):1 | ||||
| chr16:30748102-30748452 | Common:2; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30768811-30769259 | Rare:136 | ||||
| chr16:30787146-30787279 | Rare:19 | ||||
| chr16:30893939-30894289 | Common:5; Rare:93 |