| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98515431-98515604 | Rare:54 | ||||
| chr12:98644737-98644853 | Common:1; Rare:39 | ||||
| chr12:98645034-98645321 | Common:2; Rare:80 | ||||
| chr12:100267045-100267279 | Common:1; Rare:115 | ||||
| chr12:100573501-100573740 | Rare:75 | ||||
| chr12:101407731-101408045 | Common:2; Rare:77 | ||||
| chr12:101594738-101595094 | Common:4; Rare:69; Clinvar (benign):5 | ||||
| chr12:102120065-102120249 | Rare:70 | ||||
| chr12:102480415-102480584 | Rare:23 | ||||
| chr12:103587104-103587278 | Rare:44 | ||||
| chr12:103930043-103930551 | Common:8; Rare:172 | ||||
| chr12:103965664-103965941 | Common:2; Rare:73 | ||||
| chr12:104064345-104064557 | Common:1; Rare:51 | ||||
| chr12:104138164-104138415 | Common:1; Rare:73 | ||||
| chr12:105107612-105107795 | Common:1; Rare:84 |