| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22814794-22814928 | Rare:50 | ||||
| chr16:23302254-23302414 | Rare:29; Clinvar (benign):1 | ||||
| chr16:23452719-23452824 | Rare:41; Clinvar (benign):1 | ||||
| chr16:23453109-23453231 | Rare:37 | ||||
| chr16:23557313-23557581 | Common:3; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641212-23641551 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24539375-24539637 | Common:1; Rare:99 | ||||
| chr16:24729604-24729758 | Common:7; Rare:78 | ||||
| chr16:25015223-25015461 | Common:2; Rare:74 | ||||
| chr16:25111474-25111852 | Common:2; Rare:111 | ||||
| chr16:27268719-27268902 | Common:1; Rare:67 | ||||
| chr16:27313789-27313993 | Common:2; Rare:58 | ||||
| chr16:27549882-27550173 | Common:2; Rare:111 | ||||
| chr16:28491928-28492121 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:28494297-28494676 | Common:1; Rare:75 |