| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98515332-98515814 | Common:1; Rare:162; Clinvar:4 | ||||
| chr12:98515817-98515894 | Rare:33; Clinvar (benign):1 | ||||
| chr12:98593467-98593776 | Common:2; Rare:100; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644703-98645307 | Common:7; Rare:176 | ||||
| chr12:99984690-99985024 | Common:3; Rare:112 | ||||
| chr12:100142816-100143010 | Common:2; Rare:80 | ||||
| chr12:100199792-100200071 | Common:1; Rare:63 | ||||
| chr12:100200707-100200866 | Rare:51 | ||||
| chr12:100266973-100267320 | Common:2; Rare:157 | ||||
| chr12:100573522-100573770 | Rare:81 | ||||
| chr12:101280020-101280207 | Common:1; Rare:56 | ||||
| chr12:101407710-101408089 | Common:3; Rare:94 | ||||
| chr12:102061958-102062184 | Rare:64 | ||||
| chr12:102120041-102120261 | Rare:88 | ||||
| chr12:102957449-102957745 | Common:4; Rare:70 |