| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30762080-30762357 | Common:3; Rare:93 | ||||
| chr16:30893940-30894275 | Common:5; Rare:91 | ||||
| chr16:30923251-30923581 | Common:1; Rare:81 | ||||
| chr16:30949186-30949321 | Common:2; Rare:42 | ||||
| chr16:30997280-30997414 | Common:1; Rare:33 | ||||
| chr16:31033236-31033596 | Common:2; Rare:106 | ||||
| chr16:31073726-31073848 | Rare:37 | ||||
| chr16:31074172-31074456 | Common:2; Rare:81 | ||||
| chr16:31094628-31094885 | Common:1; Rare:90; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:31202694-31202833 | Common:1; Rare:58 | ||||
| chr16:31442763-31443059 | Common:1; Rare:48 | ||||
| chr16:31471896-31472198 | Rare:69 | ||||
| chr16:31508374-31508516 | Common:4; Rare:58 | ||||
| chr16:46689135-46689277 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689518-46689700 | Common:2; Rare:76; Clinvar (benign):2 |