| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:88141960-88142427 | Rare:132; Clinvar:6 | ||||
| chr12:88580044-88580307 | Common:1; Rare:67; Clinvar (benign):1 | ||||
| chr12:88580382-88580622 | Common:2; Rare:73 | ||||
| chr12:89351697-89351912 | Common:2; Rare:73 | ||||
| chr12:89353400-89353564 | Rare:39 | ||||
| chr12:89353629-89353786 | Common:3; Rare:36 | ||||
| chr12:89461805-89462157 | Rare:47 | ||||
| chr12:89524734-89524952 | Common:2; Rare:53 | ||||
| chr12:89525423-89525651 | Common:1; Rare:58 | ||||
| chr12:89525968-89526067 | Rare:42 | ||||
| chr12:89526167-89526336 | Rare:34 | ||||
| chr12:89708745-89709125 | Common:1; Rare:144 | ||||
| chr12:89709155-89709470 | Common:4; Rare:125 | ||||
| chr12:89709505-89709578 | Rare:27 | ||||
| chr12:89709598-89709867 | Common:1; Rare:101 |