| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53268169-53268332 | Common:1; Rare:41 | ||||
| chr12:53268431-53268592 | Rare:28 | ||||
| chr12:53295352-53295640 | Common:2; Rare:95 | ||||
| chr12:53295765-53295831 | Rare:23 | ||||
| chr12:53295872-53295949 | Rare:27 | ||||
| chr12:53299629-53300091 | Common:2; Rare:206 | ||||
| chr12:53300326-53300456 | Common:1; Rare:24 | ||||
| chr12:53320816-53320980 | Rare:28 | ||||
| chr12:53321226-53321724 | Common:2; Rare:160; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr12:53324218-53324313 | Rare:17 | ||||
| chr12:53324720-53325178 | Common:1; Rare:99 | ||||
| chr12:53325194-53325305 | Rare:13 | ||||
| chr12:53325313-53325372 | Common:1; Rare:12 | ||||
| chr12:53344871-53344975 | Rare:23 | ||||
| chr12:53380107-53380269 | Common:3; Rare:71 |