| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95858830-95859061 | Common:3; Rare:70 | ||||
| chr12:96400550-96400875 | Rare:105 | ||||
| chr12:96907174-96907285 | Rare:41 | ||||
| chr12:98515475-98516069 | Rare:207; Clinvar:10; Clinvar (benign):4 | ||||
| chr12:98593474-98593767 | Common:2; Rare:98; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644982-98645296 | Common:2; Rare:93 | ||||
| chr12:99984642-99985014 | Common:2; Rare:128 | ||||
| chr12:100200717-100200851 | Rare:44 | ||||
| chr12:100267047-100267440 | Common:2; Rare:162 | ||||
| chr12:100573609-100573700 | Rare:22 | ||||
| chr12:101407678-101408049 | Common:3; Rare:88 | ||||
| chr12:101697425-101697918 | Common:4; Rare:155 | ||||
| chr12:101877519-101877762 | Common:3; Rare:64 | ||||
| chr12:102120060-102120254 | Rare:77 | ||||
| chr12:103930077-103930554 | Common:8; Rare:163 |