| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:16223458-16223559 | Rare:9 | ||||
| chr16:18801448-18801708 | Common:2; Rare:101 | ||||
| chr16:19067455-19067696 | Common:5; Rare:101; Clinvar:1 | ||||
| chr16:19067808-19067917 | Common:2; Rare:27 | ||||
| chr16:19410292-19410602 | Common:3; Rare:50 | ||||
| chr16:19521995-19522141 | Rare:42 | ||||
| chr16:19523556-19523963 | Common:4; Rare:75 | ||||
| chr16:19555573-19555729 | Common:1; Rare:83 | ||||
| chr16:20763937-20764064 | Common:2; Rare:21 | ||||
| chr16:20806331-20806659 | Rare:103 | ||||
| chr16:20900301-20900792 | Common:3; Rare:108 | ||||
| chr16:21599438-21599763 | Common:4; Rare:113 | ||||
| chr16:21652602-21652708 | Rare:27 | ||||
| chr16:21953038-21953413 | Common:1; Rare:96; Clinvar (benign):3 | ||||
| chr16:22206556-22206676 | Rare:23 |