| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88733056-88733320 | Common:2; Rare:98 | ||||
| chr16:88785217-88785398 | Common:1; Rare:55 | ||||
| chr16:88811885-88811970 | Common:1; Rare:53; Clinvar (benign):1 | ||||
| chr16:88856896-88857186 | Common:4; Rare:144; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:88857877-88858142 | Common:2; Rare:54 | ||||
| chr16:89217619-89217765 | Common:1; Rare:72 | ||||
| chr16:89489374-89489479 | Rare:29 | ||||
| chr16:89508310-89508548 | Common:2; Rare:116; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr16:89544246-89544331 | Rare:15 | ||||
| chr16:89560465-89560764 | Common:1; Rare:144 | ||||
| chr16:89657580-89658156 | Common:5; Rare:281; Clinvar (benign):1 | ||||
| chr16:89686898-89687022 | Rare:54 | ||||
| chr16:89701623-89701807 | Common:1; Rare:66 | ||||
| chr16:89711698-89711906 | Common:3; Rare:85 | ||||
| chr16:89719026-89719356 | Common:3; Rare:140 |