| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96907139-96907295 | Common:1; Rare:55 | ||||
| chr12:98515435-98515759 | Rare:104; Clinvar:2 | ||||
| chr12:98515772-98515814 | Rare:14; Clinvar:2 | ||||
| chr12:98515836-98516134 | Common:2; Rare:117; Clinvar:7; Clinvar (benign):10 | ||||
| chr12:98593467-98593771 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644703-98644843 | Common:3; Rare:47 | ||||
| chr12:98644938-98645307 | Common:2; Rare:107 | ||||
| chr12:100267047-100267246 | Common:1; Rare:103 | ||||
| chr12:100573554-100573761 | Rare:72 | ||||
| chr12:101407697-101408056 | Common:3; Rare:85 | ||||
| chr12:101877621-101877797 | Common:4; Rare:47 | ||||
| chr12:102120065-102120265 | Rare:80 | ||||
| chr12:103930044-103930529 | Common:8; Rare:163 | ||||
| chr12:103957147-103957335 | Common:5; Rare:55 | ||||
| chr12:103965705-103965941 | Common:2; Rare:55 |