| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89686910-89687056 | Common:2; Rare:63 | ||||
| chr16:89711642-89711896 | Common:3; Rare:95 | ||||
| chr16:89720865-89721003 | Common:1; Rare:40 | ||||
| chr16:89816576-89816760 | Common:4; Rare:99; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr16:89873441-89873715 | Common:4; Rare:125 | ||||
| chr16:89921793-89921898 | Rare:35 | ||||
| chr16:89923171-89923352 | Rare:65 | ||||
| chr16:89948560-89948809 | Common:3; Rare:75 | ||||
| chr16:89958077-89958387 | Common:2; Rare:67 | ||||
| chr16:89972478-89972900 | Common:3; Rare:159 | ||||
| chr16:90019355-90019681 | Common:6; Rare:100 | ||||
| chr16:90019684-90019770 | Rare:28 | ||||
| chr16:90019835-90019960 | Rare:35 | ||||
| chr16:90022533-90022713 | Rare:71 | ||||
| chr17:352710-353226 | Common:8; Rare:108 |