| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:85898983-85899223 | Common:4; Rare:71 | ||||
| chr16:85902710-85903083 | Common:1; Rare:103; Clinvar:1 | ||||
| chr16:86555155-86555264 | Rare:60 | ||||
| chr16:87317394-87317516 | Common:2; Rare:45 | ||||
| chr16:87765914-87766068 | Common:1; Rare:62 | ||||
| chr16:88570159-88570482 | Common:2; Rare:122 | ||||
| chr16:88599236-88599539 | Common:1; Rare:71 | ||||
| chr16:88649830-88649860 | Rare:3 | ||||
| chr16:88650922-88651174 | Common:1; Rare:83; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:88663058-88663374 | Common:8; Rare:131 | ||||
| chr16:88686378-88686620 | Common:4; Rare:112 | ||||
| chr16:88703565-88703774 | Common:3; Rare:67 | ||||
| chr16:88706252-88706538 | Common:4; Rare:137 | ||||
| chr16:88719710-88719812 | Rare:48 | ||||
| chr16:88725447-88725737 | Common:3; Rare:143; Clinvar (benign):2 |