| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:82169858-82170000 | Common:4; Rare:90 | ||||
| chr16:82170065-82170465 | Common:26; Rare:586 | ||||
| chr16:83807677-83808095 | Common:7; Rare:364 | ||||
| chr16:83808228-83808912 | Common:3; Rare:321 | ||||
| chr16:83898825-83899225 | Common:10; Rare:385; Clinvar:3; Clinvar (benign):28 | ||||
| chr16:83899410-83899860 | Common:5; Rare:342; Clinvar:8; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr16:83952957-83953371 | Common:7; Rare:445 | ||||
| chr16:83953460-83953800 | Common:7; Rare:183 | ||||
| chr16:83968480-83968940 | Common:3; Rare:155 | ||||
| chr16:84043035-84043490 | Common:3; Rare:235 | ||||
| chr16:84116100-84116480 | Common:5; Rare:218 | ||||
| chr16:84116651-84117136 | Common:29; Rare:930 | ||||
| chr16:84117336-84117736 | Common:1; Rare:116 | ||||
| chr16:84143852-84144842 | Common:10; Rare:454 | ||||
| chr16:84145060-84145460 | Common:8; Rare:415; Clinvar:14; Clinvar (benign):2 |