| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:27549897-27550149 | Common:2; Rare:87 | ||||
| chr16:28846281-28846646 | Common:2; Rare:122; Clinvar:5; Clinvar (benign):4 | ||||
| chr16:30075883-30076040 | Rare:53 | ||||
| chr16:30762090-30762324 | Common:3; Rare:83 | ||||
| chr16:47461046-47461333 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr16:53703825-53704203 | Common:1; Rare:116; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:56451312-56451551 | Common:1; Rare:62 | ||||
| chr16:56729977-56730189 | Common:1; Rare:48 | ||||
| chr16:57185997-57186333 | Common:1; Rare:97 | ||||
| chr16:57447360-57447493 | Common:2; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:58129310-58129567 | Common:2; Rare:81 | ||||
| chr16:66934373-66934457 | Rare:36 | ||||
| chr16:67227020-67227163 | Rare:56 | ||||
| chr16:67481136-67481396 | Common:1; Rare:86 | ||||
| chr16:68310934-68311019 | Rare:36 |