| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67966792-67966970 | Rare:36 | ||||
| chr16:67968539-67968856 | Common:2; Rare:109 | ||||
| chr16:68023209-68023314 | Common:1; Rare:28 | ||||
| chr16:68245187-68245402 | Common:1; Rare:67 | ||||
| chr16:68310915-68311081 | Common:1; Rare:83 | ||||
| chr16:69132532-69132680 | Rare:61 | ||||
| chr16:69339548-69339826 | Common:1; Rare:116; Clinvar (benign):1 | ||||
| chr16:69726403-69726850 | Common:4; Rare:123 | ||||
| chr16:70114127-70114373 | Common:3; Rare:88 | ||||
| chr16:70289434-70289802 | Common:3; Rare:147; Clinvar:1 | ||||
| chr16:70346759-70346982 | Common:2; Rare:110 | ||||
| chr16:70523532-70523855 | Common:3; Rare:105; Clinvar (pathogenic):1 | ||||
| chr16:71808772-71808869 | Common:1; Rare:53 | ||||
| chr16:71809010-71809134 | Rare:48 | ||||
| chr16:71845904-71846017 | Common:2; Rare:35 |