| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89712484-89712758 | Common:4; Rare:122 | ||||
| chr16:89719377-89719540 | Common:3; Rare:55 | ||||
| chr16:89720342-89720464 | Common:2; Rare:35 | ||||
| chr16:89720849-89721210 | Common:3; Rare:110 | ||||
| chr16:89721227-89721587 | Common:3; Rare:149 | ||||
| chr16:89721679-89721982 | Rare:101 | ||||
| chr16:89816454-89816928 | Common:9; Rare:240; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
| chr16:89816940-89817091 | Common:1; Rare:76 | ||||
| chr16:89828333-89828525 | Rare:82 | ||||
| chr16:89873226-89873277 | Rare:10 | ||||
| chr16:89873342-89873714 | Common:5; Rare:157 | ||||
| chr16:89873809-89873900 | Common:4; Rare:32 | ||||
| chr16:89874031-89874493 | Common:5; Rare:134 | ||||
| chr16:89917848-89917917 | Rare:14 | ||||
| chr16:89917993-89918162 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):2 |