| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98515430-98515902 | Rare:169; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:98545050-98545110 | Rare:15 | ||||
| chr12:98593565-98594131 | Common:1; Rare:196; Clinvar:7; Clinvar (benign):7 | ||||
| chr12:98597099-98597404 | Rare:48 | ||||
| chr12:98644532-98644654 | Rare:47 | ||||
| chr12:98644697-98644834 | Common:3; Rare:47 | ||||
| chr12:98644912-98645296 | Common:4; Rare:111 | ||||
| chr12:100142847-100142994 | Common:2; Rare:55 | ||||
| chr12:100200690-100200863 | Rare:56 | ||||
| chr12:100266993-100267434 | Common:3; Rare:187 | ||||
| chr12:100573554-100573767 | Rare:73 | ||||
| chr12:101407643-101408035 | Common:3; Rare:97 | ||||
| chr12:102074856-102075161 | Common:1; Rare:69 | ||||
| chr12:102120045-102120269 | Common:1; Rare:91 | ||||
| chr12:103841180-103841492 | Common:5; Rare:115 |