| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:99710427-99710759 | Common:1; Rare:101 | ||||
| chr15:99806858-99806997 | Common:2; Rare:20 | ||||
| chr15:100895725-100896006 | Common:2; Rare:63; Clinvar (benign):1 | ||||
| chr15:101961567-101961633 | Rare:2 | ||||
| chr16:264661-264858 | Common:2; Rare:83 | ||||
| chr16:377076-377459 | Common:6; Rare:174 | ||||
| chr16:518722-519018 | Common:3; Rare:75 | ||||
| chr16:528826-528952 | Rare:33 | ||||
| chr16:1349926-1350073 | Common:1; Rare:70 | ||||
| chr16:1361814-1361905 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:1362045-1362258 | Rare:98; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr16:1511050-1511251 | Common:1; Rare:94; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:2037504-2037622 | Common:1; Rare:50 | ||||
| chr16:2086549-2086860 | Common:2; Rare:112; Clinvar:14; Clinvar (benign):26; Clinvar (pathogenic):1 | ||||
| chr16:2663452-2663646 | Rare:45 |