| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:101652117-101652810 | Common:7; Rare:256 | ||||
| chr15:101652851-101652994 | Rare:48 | ||||
| chr15:101724048-101724261 | Common:1; Rare:72 | ||||
| chr16:52961-53397 | Common:2; Rare:95 | ||||
| chr16:53448-53929 | Common:9; Rare:170 | ||||
| chr16:72573-72786 | Common:8; Rare:51 | ||||
| chr16:72828-72918 | Common:2; Rare:13 | ||||
| chr16:76772-77062 | Common:4; Rare:54 | ||||
| chr16:77360-77644 | Common:1; Rare:59 | ||||
| chr16:77683-77787 | Common:3; Rare:27 | ||||
| chr16:77966-78336 | Common:5; Rare:124 | ||||
| chr16:78483-78643 | Common:1; Rare:31 | ||||
| chr16:138143-138253 | Rare:25; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:138590-138910 | Common:14; Rare:103 | ||||
| chr16:228707-228804 | Rare:36 |