| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30526398-30526917 | Common:9; Rare:263 | ||||
| chr16:30534651-30535105 | Common:6; Rare:226 | ||||
| chr16:30558324-30558610 | Common:6; Rare:119 | ||||
| chr16:30571480-30571887 | Rare:201 | ||||
| chr16:30572154-30572265 | Rare:34 | ||||
| chr16:30610246-30610568 | Common:2; Rare:154 | ||||
| chr16:30650582-30650798 | Rare:80 | ||||
| chr16:30650800-30651002 | Rare:120 | ||||
| chr16:30651220-30651750 | Rare:214 | ||||
| chr16:30658030-30658504 | Common:2; Rare:206 | ||||
| chr16:30658589-30658864 | Common:2; Rare:164 | ||||
| chr16:30698008-30698271 | Common:1; Rare:207 | ||||
| chr16:30698431-30698727 | Common:2; Rare:199 | ||||
| chr16:30698972-30699402 | Rare:227; Clinvar (benign):2 | ||||
| chr16:30748086-30748475 | Common:4; Rare:181; Clinvar:4; Clinvar (benign):2 |