| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69132528-69132680 | Rare:61 | ||||
| chr16:69311106-69311435 | Rare:102 | ||||
| chr16:69339551-69339840 | Common:1; Rare:124; Clinvar (benign):1 | ||||
| chr16:69424366-69424707 | Common:2; Rare:93 | ||||
| chr16:69565635-69565951 | Common:4; Rare:109 | ||||
| chr16:69726379-69726513 | Common:2; Rare:53 | ||||
| chr16:69726531-69726785 | Common:3; Rare:58 | ||||
| chr16:69754875-69755089 | Rare:85 | ||||
| chr16:69762201-69762582 | Common:3; Rare:130 | ||||
| chr16:69890591-69890817 | Common:1; Rare:44 | ||||
| chr16:70114105-70114409 | Common:3; Rare:102 | ||||
| chr16:70289419-70289767 | Common:3; Rare:140; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:70299071-70299277 | Common:1; Rare:44 | ||||
| chr16:70346751-70346971 | Common:2; Rare:109 | ||||
| chr16:70454324-70454638 | Common:2; Rare:85 |