| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30787157-30787416 | Common:1; Rare:48 | ||||
| chr16:30893966-30894275 | Common:5; Rare:81 | ||||
| chr16:30896402-30896624 | Common:2; Rare:51 | ||||
| chr16:30923236-30923592 | Common:1; Rare:87 | ||||
| chr16:31033434-31033601 | Common:1; Rare:64 | ||||
| chr16:31073726-31073821 | Rare:28 | ||||
| chr16:31074187-31074450 | Common:1; Rare:73 | ||||
| chr16:31202703-31202879 | Common:2; Rare:66 | ||||
| chr16:31442763-31443059 | Common:1; Rare:48 | ||||
| chr16:31458897-31459202 | Rare:86 | ||||
| chr16:31459297-31459527 | Common:1; Rare:95 | ||||
| chr16:31471931-31472194 | Rare:62 | ||||
| chr16:31508351-31508509 | Common:4; Rare:70 | ||||
| chr16:46689134-46689317 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689504-46689708 | Common:2; Rare:83; Clinvar (benign):2; Clinvar (pathogenic):1 |