| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88706315-88706535 | Common:4; Rare:109 | ||||
| chr16:88811888-88811985 | Common:2; Rare:56; Clinvar (benign):1 | ||||
| chr16:88856921-88857163 | Common:4; Rare:110; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89217619-89217749 | Common:1; Rare:61 | ||||
| chr16:89508325-89508468 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560526-89560763 | Rare:109 | ||||
| chr16:89657644-89658095 | Common:3; Rare:236 | ||||
| chr16:89686596-89686706 | Common:6; Rare:55 | ||||
| chr16:89686889-89686999 | Rare:47 | ||||
| chr16:89720865-89721006 | Common:1; Rare:41 | ||||
| chr16:89816618-89816758 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:89873492-89873658 | Common:1; Rare:79 | ||||
| chr16:89921774-89921944 | Rare:54 | ||||
| chr16:89923171-89923356 | Rare:68 | ||||
| chr16:89948560-89948803 | Common:3; Rare:72 |