| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67481088-67481404 | Common:1; Rare:118 | ||||
| chr16:67528661-67528883 | Rare:58 | ||||
| chr16:67660222-67660391 | Rare:105; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67660761-67661062 | Common:2; Rare:105 | ||||
| chr16:67719278-67719460 | Rare:49 | ||||
| chr16:67846713-67846976 | Common:1; Rare:70 | ||||
| chr16:67935662-67935959 | Common:1; Rare:96 | ||||
| chr16:67936809-67936885 | Rare:13 | ||||
| chr16:67951480-67951558 | Rare:17 | ||||
| chr16:67968573-67968863 | Common:2; Rare:96 | ||||
| chr16:68023209-68023302 | Common:1; Rare:25 | ||||
| chr16:68245129-68245402 | Common:1; Rare:80 | ||||
| chr16:68310865-68311148 | Common:3; Rare:142 | ||||
| chr16:68539149-68539379 | Common:2; Rare:103 | ||||
| chr16:68843488-68843550 | Rare:15 |