| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95790803-95790952 | Common:2; Rare:53 | ||||
| chr12:95858873-95859076 | Common:1; Rare:62 | ||||
| chr12:96194208-96194578 | Common:5; Rare:122 | ||||
| chr12:96399371-96399461 | Common:1; Rare:25 | ||||
| chr12:96400047-96400305 | Common:1; Rare:69 | ||||
| chr12:96400550-96400710 | Rare:75 | ||||
| chr12:96907174-96907295 | Rare:44 | ||||
| chr12:98515353-98515648 | Common:1; Rare:100; Clinvar:1 | ||||
| chr12:98515866-98515880 | Rare:2 | ||||
| chr12:98593449-98594406 | Common:3; Rare:337; Clinvar:7; Clinvar (benign):7 | ||||
| chr12:98644711-98645325 | Common:7; Rare:178 | ||||
| chr12:100200714-100200857 | Rare:47 | ||||
| chr12:100267047-100267449 | Common:3; Rare:166 | ||||
| chr12:100573557-100573770 | Rare:73 | ||||
| chr12:101280029-101280143 | Common:1; Rare:34 |