| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4693387-4693771 | Common:3; Rare:165 | ||||
| chr16:4694101-4694236 | Rare:66 | ||||
| chr16:4733920-4733950 | Rare:5 | ||||
| chr16:4734071-4734603 | Common:2; Rare:198 | ||||
| chr16:4734807-4734984 | Rare:55 | ||||
| chr16:4767111-4767441 | Common:3; Rare:101 | ||||
| chr16:4788645-4788830 | Rare:45 | ||||
| chr16:4802112-4802452 | Common:1; Rare:176; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:4802601-4802890 | Rare:106; Clinvar:5 | ||||
| chr16:4846609-4846733 | Common:2; Rare:33 | ||||
| chr16:4847054-4847068 | Rare:2 | ||||
| chr16:4847221-4847750 | Common:3; Rare:235 | ||||
| chr16:4847852-4848003 | Common:2; Rare:49 | ||||
| chr16:4848201-4848489 | Common:4; Rare:78 | ||||
| chr16:4937096-4937468 | Common:6; Rare:120 |