| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98515494-98515814 | Rare:100; Clinvar:4 | ||||
| chr12:98593469-98593790 | Common:2; Rare:103; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644646-98644843 | Common:3; Rare:70 | ||||
| chr12:98644925-98645307 | Common:4; Rare:112 | ||||
| chr12:100200710-100200876 | Rare:53 | ||||
| chr12:100267045-100267303 | Common:1; Rare:118 | ||||
| chr12:101407653-101408076 | Common:3; Rare:108 | ||||
| chr12:101877502-101877755 | Common:3; Rare:68 | ||||
| chr12:102061958-102062194 | Rare:65 | ||||
| chr12:102120041-102120274 | Common:1; Rare:93 | ||||
| chr12:103841256-103841488 | Common:3; Rare:80 | ||||
| chr12:103930026-103930557 | Common:9; Rare:178 | ||||
| chr12:103965722-103965941 | Common:2; Rare:51 | ||||
| chr12:104064451-104064555 | Rare:27 | ||||
| chr12:104138147-104138426 | Common:1; Rare:79 |