| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89701510-89701736 | Common:2; Rare:74 | ||||
| chr16:89701958-89702266 | Common:9; Rare:97 | ||||
| chr16:89711815-89711949 | Rare:67 | ||||
| chr16:89712034-89712114 | Rare:30 | ||||
| chr16:89712479-89712630 | Common:3; Rare:74 | ||||
| chr16:89719369-89719645 | Common:4; Rare:83 | ||||
| chr16:89720681-89721139 | Common:3; Rare:142 | ||||
| chr16:89721146-89721709 | Common:3; Rare:224 | ||||
| chr16:89721929-89722071 | Common:1; Rare:41 | ||||
| chr16:89722633-89722891 | Common:1; Rare:119 | ||||
| chr16:89816561-89816949 | Common:8; Rare:201; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr16:89816961-89817085 | Common:1; Rare:65 | ||||
| chr16:89828254-89828592 | Common:4; Rare:136 | ||||
| chr16:89872884-89873235 | Common:4; Rare:91 | ||||
| chr16:89873237-89873376 | Common:1; Rare:36 |