| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31072528-31072767 | Rare:40 | ||||
| chr16:31073160-31073480 | Common:2; Rare:94 | ||||
| chr16:31073679-31073848 | Rare:101 | ||||
| chr16:31074172-31074485 | Common:4; Rare:169 | ||||
| chr16:31094562-31095040 | Common:2; Rare:246; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr16:31108273-31108507 | Rare:95 | ||||
| chr16:31117879-31118019 | Rare:36 | ||||
| chr16:31179816-31180210 | Common:3; Rare:172; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31180596-31180871 | Common:6; Rare:197 | ||||
| chr16:31458090-31458356 | Common:1; Rare:63 | ||||
| chr16:31458869-31459172 | Common:1; Rare:118 | ||||
| chr16:31459247-31459519 | Common:2; Rare:209 | ||||
| chr16:31471907-31472186 | Rare:64 | ||||
| chr16:31484370-31484770 | Common:5; Rare:150; Clinvar (pathogenic):2 | ||||
| chr16:31508010-31508517 | Common:12; Rare:354 |