| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30069595-30069918 | Common:1; Rare:120; Clinvar:4; Clinvar (benign):6 | ||||
| chr16:30355219-30355422 | Common:1; Rare:74 | ||||
| chr16:30534830-30535113 | Common:3; Rare:92 | ||||
| chr16:31471950-31472181 | Rare:51 | ||||
| chr16:46689131-46689386 | Common:1; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689521-46689740 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:47461051-47461359 | Common:2; Rare:109; Clinvar (benign):2 | ||||
| chr16:53703825-53704206 | Common:1; Rare:117; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:56451114-56451662 | Common:4; Rare:182 | ||||
| chr16:56608233-56608760 | Common:4; Rare:146 | ||||
| chr16:56931923-56932156 | Common:1; Rare:113 | ||||
| chr16:57185984-57186335 | Common:1; Rare:100 | ||||
| chr16:57447344-57447544 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:66366389-66366730 | Common:3; Rare:76 | ||||
| chr16:66604406-66604802 | Rare:100 |