| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30787150-30787225 | Rare:12 | ||||
| chr16:30893966-30894147 | Common:4; Rare:43 | ||||
| chr16:30897021-30897383 | Common:1; Rare:57 | ||||
| chr16:30922737-30922926 | Common:1; Rare:55 | ||||
| chr16:30923142-30923626 | Common:1; Rare:132 | ||||
| chr16:30948937-30949163 | Rare:41 | ||||
| chr16:30957028-30957287 | Common:3; Rare:52 | ||||
| chr16:30957500-30958010 | Common:1; Rare:155 | ||||
| chr16:30996933-30997447 | Common:1; Rare:108; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:31032738-31033047 | Common:1; Rare:58 | ||||
| chr16:31033158-31033625 | Common:2; Rare:131 | ||||
| chr16:31034247-31034328 | Rare:26 | ||||
| chr16:31073193-31073530 | Common:2; Rare:97 | ||||
| chr16:31073621-31073896 | Rare:80 | ||||
| chr16:31074123-31074565 | Common:3; Rare:124 |