| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30748105-30748462 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762052-30762343 | Common:3; Rare:93 | ||||
| chr16:30893940-30894268 | Common:5; Rare:88 | ||||
| chr16:30923242-30923608 | Common:1; Rare:88 | ||||
| chr16:31033218-31033606 | Common:2; Rare:114 | ||||
| chr16:31073722-31073848 | Rare:39 | ||||
| chr16:31074187-31074456 | Common:1; Rare:75 | ||||
| chr16:31442779-31443059 | Common:1; Rare:46 | ||||
| chr16:31472109-31472194 | Rare:25 | ||||
| chr16:31508365-31508472 | Common:1; Rare:45 | ||||
| chr16:46689130-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689504-46689724 | Common:2; Rare:92; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973561-46973775 | Rare:92 | ||||
| chr16:47461027-47461374 | Common:2; Rare:135; Clinvar (benign):2 | ||||
| chr16:48244240-48244508 | Common:2; Rare:82 |