| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89816561-89817042 | Common:8; Rare:249; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr16:89863828-89864253 | Common:4; Rare:107 | ||||
| chr16:89873378-89873678 | Common:4; Rare:140 | ||||
| chr16:89873809-89873926 | Common:4; Rare:41 | ||||
| chr16:89874044-89874455 | Common:5; Rare:120 | ||||
| chr16:89917928-89918194 | Common:3; Rare:82; Clinvar:5; Clinvar (benign):4 | ||||
| chr16:89918288-89918315 | Rare:9 | ||||
| chr16:89923171-89923381 | Rare:93 | ||||
| chr16:89948087-89948368 | Common:12; Rare:82 | ||||
| chr16:89948655-89948801 | Common:2; Rare:38 | ||||
| chr16:89972414-89972693 | Common:1; Rare:104 | ||||
| chr16:89972777-89972921 | Common:2; Rare:57 | ||||
| chr16:90008941-90009162 | Common:4; Rare:48 | ||||
| chr16:90019446-90019676 | Common:4; Rare:72 | ||||
| chr16:90022524-90022697 | Rare:66 |