| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12717530-12717930 | Common:1; Rare:157; Clinvar:11; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr12:12718336-12718736 | Common:1; Rare:128 | ||||
| chr12:12725140-12725550 | Common:9; Rare:255 | ||||
| chr12:12725561-12726164 | Common:25; Rare:582 | ||||
| chr12:12813099-12813499 | Common:6; Rare:284 | ||||
| chr12:12891323-12891723 | Common:3; Rare:125 | ||||
| chr12:13000070-13000550 | Common:12; Rare:575 | ||||
| chr12:13044160-13044520 | Rare:117 | ||||
| chr12:14365367-14365767 | Common:6; Rare:522 | ||||
| chr12:14365794-14366194 | Rare:202 | ||||
| chr12:14367056-14367804 | Common:4; Rare:263 | ||||
| chr12:14384811-14385320 | Common:7; Rare:249 | ||||
| chr12:14385255-14385409 | Rare:52 | ||||
| chr12:14385386-14385786 | Common:3; Rare:74 | ||||
| chr12:14394369-14394850 | Common:1; Rare:137 |