| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95474043-95474191 | Common:2; Rare:69 | ||||
| chr12:95858822-95859075 | Common:3; Rare:74 | ||||
| chr12:96400559-96400673 | Rare:52 | ||||
| chr12:96489449-96489598 | Common:2; Rare:34 | ||||
| chr12:96907180-96907282 | Rare:38 | ||||
| chr12:98515428-98515697 | Rare:90; Clinvar:1 | ||||
| chr12:98593484-98593765 | Common:2; Rare:97; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644731-98645293 | Common:5; Rare:161 | ||||
| chr12:99154745-99154912 | Rare:32 | ||||
| chr12:100200553-100200862 | Common:3; Rare:91 | ||||
| chr12:100267063-100267326 | Common:1; Rare:109 | ||||
| chr12:100573601-100573740 | Rare:42 | ||||
| chr12:101280025-101280143 | Common:1; Rare:36 | ||||
| chr12:101407690-101408099 | Common:3; Rare:103 | ||||
| chr12:102061958-102062193 | Rare:64 |