| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74701089-74701344 | Common:2; Rare:50 | ||||
| chr16:75248123-75248365 | Common:2; Rare:62 | ||||
| chr16:75306388-75306547 | Rare:26 | ||||
| chr16:75464380-75464490 | Common:2; Rare:57 | ||||
| chr16:75556218-75556534 | Common:1; Rare:98; Clinvar (benign):3 | ||||
| chr16:75647614-75647861 | Common:4; Rare:125; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648092-75648263 | Rare:69 | ||||
| chr16:77190686-77191021 | Common:10; Rare:109 | ||||
| chr16:77191136-77191252 | Common:1; Rare:49 | ||||
| chr16:77722314-77722541 | Common:3; Rare:70 | ||||
| chr16:81006430-81006576 | Rare:46 | ||||
| chr16:81006825-81007277 | Common:3; Rare:152 | ||||
| chr16:82034965-82035442 | Common:2; Rare:117 | ||||
| chr16:84116796-84117101 | Common:3; Rare:125 | ||||
| chr16:84504608-84504944 | Common:11; Rare:142 |