| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30896512-30896738 | Common:1; Rare:56 | ||||
| chr16:30923246-30923610 | Common:1; Rare:88 | ||||
| chr16:30948775-30949130 | Rare:71 | ||||
| chr16:30956990-30957306 | Common:3; Rare:69 | ||||
| chr16:30958218-30958330 | Common:2; Rare:28 | ||||
| chr16:30985048-30985273 | Rare:63 | ||||
| chr16:31032802-31032949 | Common:1; Rare:23 | ||||
| chr16:31033343-31033665 | Common:2; Rare:102 | ||||
| chr16:31033683-31033830 | Rare:37 | ||||
| chr16:31033926-31034127 | Rare:61 | ||||
| chr16:31065007-31065251 | Rare:40 | ||||
| chr16:31073701-31073816 | Rare:35 | ||||
| chr16:31074175-31074457 | Common:2; Rare:79 | ||||
| chr16:31093371-31093663 | Common:2; Rare:67; Clinvar (benign):1 | ||||
| chr16:31094555-31094648 | Rare:31; Clinvar (pathogenic):2 |