| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:82169879-82169998 | Common:2; Rare:43 | ||||
| chr16:82170060-82170445 | Common:11; Rare:192 | ||||
| chr16:82170524-82170648 | Common:3; Rare:33 | ||||
| chr16:82170679-82170835 | Rare:39 | ||||
| chr16:82626831-82627154 | Rare:107 | ||||
| chr16:82627282-82627440 | Common:5; Rare:46 | ||||
| chr16:82627448-82627635 | Rare:63 | ||||
| chr16:83807794-83808094 | Common:2; Rare:110 | ||||
| chr16:83808175-83808253 | Rare:33 | ||||
| chr16:83808377-83808515 | Common:1; Rare:43 | ||||
| chr16:83898910-83899219 | Common:4; Rare:136; Clinvar:1; Clinvar (benign):10 | ||||
| chr16:83899439-83899645 | Common:1; Rare:99; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr16:83952757-83952800 | Common:1; Rare:10 | ||||
| chr16:83953071-83953307 | Common:2; Rare:80 | ||||
| chr16:83953553-83953759 | Common:2; Rare:56 |