| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52010397-52010530 | Rare:21 | ||||
| chr12:52051123-52051493 | Common:1; Rare:121 | ||||
| chr12:52069933-52070048 | Common:1; Rare:41 | ||||
| chr12:53006108-53006494 | Common:4; Rare:141 | ||||
| chr12:53006882-53007049 | Rare:45 | ||||
| chr12:53079365-53079559 | Common:2; Rare:63 | ||||
| chr12:53180436-53180768 | Common:2; Rare:131 | ||||
| chr12:53180891-53181146 | Common:4; Rare:73 | ||||
| chr12:53197661-53197866 | Common:1; Rare:79 | ||||
| chr12:53251986-53252208 | Common:3; Rare:88 | ||||
| chr12:53268168-53268328 | Common:1; Rare:42 | ||||
| chr12:53295436-53295639 | Common:1; Rare:71 | ||||
| chr12:53299680-53299849 | Common:2; Rare:107 | ||||
| chr12:53306042-53306209 | Rare:51 | ||||
| chr12:53321232-53321415 | Common:1; Rare:66; Clinvar:2; Clinvar (pathogenic):1 |