| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19691182-19691384 | Common:1; Rare:53 | ||||
| chr16:20763934-20764029 | Common:2; Rare:14 | ||||
| chr16:20806373-20806632 | Rare:90 | ||||
| chr16:20900798-20900893 | Common:1; Rare:26 | ||||
| chr16:21599383-21599638 | Common:4; Rare:90 | ||||
| chr16:21599743-21599821 | Rare:34 | ||||
| chr16:21953017-21953453 | Common:1; Rare:110; Clinvar (benign):3 | ||||
| chr16:21962459-21962778 | Common:3; Rare:78; Clinvar (pathogenic):1 | ||||
| chr16:22008037-22008334 | Common:2; Rare:88 | ||||
| chr16:22206015-22206341 | Common:1; Rare:88 | ||||
| chr16:22374612-22374835 | Common:1; Rare:70 | ||||
| chr16:22436897-22437055 | Rare:46 | ||||
| chr16:22437117-22437326 | Rare:70 | ||||
| chr16:23452941-23453054 | Rare:35 | ||||
| chr16:23557223-23557562 | Common:2; Rare:134; Clinvar:1; Clinvar (benign):4 |