| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1308892-1309280 | Common:5; Rare:190 | ||||
| chr16:1309378-1309766 | Rare:270 | ||||
| chr16:1351769-1352004 | Common:4; Rare:205; Clinvar:12; Clinvar (benign):2 | ||||
| chr16:1420698-1420957 | Common:2; Rare:222 | ||||
| chr16:1474977-1475182 | Common:7; Rare:134; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:1493233-1493639 | Common:8; Rare:227 | ||||
| chr16:1610181-1610581 | Common:3; Rare:191 | ||||
| chr16:1610501-1611101 | Common:2; Rare:282; Clinvar:2 | ||||
| chr16:1611962-1612451 | Common:7; Rare:344; Clinvar:4 | ||||
| chr16:1677991-1678343 | Common:6; Rare:189 | ||||
| chr16:1706043-1706432 | Common:7; Rare:189 | ||||
| chr16:1771500-1771873 | Common:6; Rare:286 | ||||
| chr16:1772639-1772853 | Common:5; Rare:132; Clinvar (pathogenic):4 | ||||
| chr16:1773053-1773247 | Rare:125; Clinvar (pathogenic):2 | ||||
| chr16:1773410-1773650 | Common:2; Rare:206 |