| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31472109-31472186 | Rare:21 | ||||
| chr16:31487790-31487820 | Rare:9 | ||||
| chr16:31508317-31508516 | Common:4; Rare:91 | ||||
| chr16:46621348-46621474 | Rare:40 | ||||
| chr16:46689129-46689652 | Common:3; Rare:168; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46972707-46972992 | Common:1; Rare:63 | ||||
| chr16:46973537-46973801 | Rare:110 | ||||
| chr16:47460841-47461383 | Common:2; Rare:215; Clinvar (benign):2 | ||||
| chr16:48244248-48244621 | Common:2; Rare:108 | ||||
| chr16:48365880-48366090 | Common:5; Rare:64 | ||||
| chr16:48609865-48610291 | Common:2; Rare:146 | ||||
| chr16:49281771-49282062 | Common:2; Rare:89 | ||||
| chr16:50065894-50065996 | Common:2; Rare:40 | ||||
| chr16:50266513-50266590 | Rare:15 | ||||
| chr16:50681268-50681418 | Common:1; Rare:33 |