| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30698469-30698639 | Common:1; Rare:66 | ||||
| chr16:30748125-30748447 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762055-30762344 | Common:3; Rare:93 | ||||
| chr16:30787165-30787248 | Rare:12 | ||||
| chr16:30893923-30894252 | Common:5; Rare:89 | ||||
| chr16:30923251-30923592 | Common:1; Rare:84 | ||||
| chr16:30984924-30985268 | Common:1; Rare:88 | ||||
| chr16:31032869-31033095 | Common:1; Rare:46 | ||||
| chr16:31033224-31033783 | Common:2; Rare:153 | ||||
| chr16:31074184-31074451 | Common:1; Rare:73 | ||||
| chr16:31355035-31355243 | Common:1; Rare:60 | ||||
| chr16:31459288-31459512 | Common:1; Rare:93 | ||||
| chr16:31471931-31472191 | Rare:60 | ||||
| chr16:31508374-31508500 | Common:4; Rare:53 | ||||
| chr16:46689141-46689357 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):1 |