| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96400437-96400665 | Common:1; Rare:101 | ||||
| chr12:96907190-96907295 | Rare:41 | ||||
| chr12:98515332-98515823 | Common:1; Rare:168; Clinvar:5 | ||||
| chr12:98515832-98515955 | Rare:43; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:98593474-98593781 | Common:2; Rare:100; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98601039-98601272 | Rare:49; Clinvar:1 | ||||
| chr12:98644737-98644843 | Common:1; Rare:36 | ||||
| chr12:98644986-98645317 | Common:2; Rare:98 | ||||
| chr12:100200010-100200117 | Rare:27 | ||||
| chr12:100200707-100200866 | Rare:51 | ||||
| chr12:100267039-100267403 | Common:1; Rare:156 | ||||
| chr12:101407641-101408076 | Common:3; Rare:110 | ||||
| chr12:101697523-101697700 | Common:2; Rare:59 | ||||
| chr12:101757571-101757874 | Rare:66; Clinvar:2 | ||||
| chr12:101877418-101877820 | Common:5; Rare:103 |