| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68023209-68023330 | Common:1; Rare:32 | ||||
| chr16:68245129-68245417 | Common:1; Rare:86 | ||||
| chr16:68264418-68264564 | Rare:50 | ||||
| chr16:68310922-68311081 | Common:1; Rare:79 | ||||
| chr16:68539135-68539338 | Common:2; Rare:101 | ||||
| chr16:69132533-69132672 | Rare:56 | ||||
| chr16:69339562-69339821 | Common:1; Rare:103; Clinvar (benign):1 | ||||
| chr16:69424340-69424698 | Common:3; Rare:96 | ||||
| chr16:69726435-69726727 | Common:4; Rare:78 | ||||
| chr16:70114105-70114376 | Common:3; Rare:94 | ||||
| chr16:70289419-70289802 | Common:3; Rare:151; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:70299132-70299259 | Rare:28 | ||||
| chr16:70346752-70346947 | Common:1; Rare:96 | ||||
| chr16:70523532-70523864 | Common:3; Rare:107; Clinvar (pathogenic):1 | ||||
| chr16:71289389-71289691 | Common:3; Rare:101 |