| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88650960-88651180 | Common:1; Rare:72; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:88663070-88663371 | Common:8; Rare:124 | ||||
| chr16:88686463-88686629 | Common:3; Rare:57 | ||||
| chr16:88703572-88703770 | Common:3; Rare:64 | ||||
| chr16:88706283-88706543 | Common:4; Rare:124 | ||||
| chr16:88725426-88725710 | Common:3; Rare:142; Clinvar (benign):2 | ||||
| chr16:88732453-88732645 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:88856816-88857163 | Common:4; Rare:161; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:88976953-88977290 | Common:1; Rare:93 | ||||
| chr16:89198189-89198444 | Rare:82 | ||||
| chr16:89199584-89199718 | Rare:34 | ||||
| chr16:89200166-89200391 | Rare:63 | ||||
| chr16:89200814-89200851 | Common:2; Rare:6 | ||||
| chr16:89217606-89217765 | Common:1; Rare:80 | ||||
| chr16:89508296-89508428 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |