| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53231860-53232547 | Common:9; Rare:414 | ||||
| chr12:53232550-53232769 | Common:3; Rare:93 | ||||
| chr12:53232764-53233252 | Common:4; Rare:190 | ||||
| chr12:53251219-53251754 | Common:4; Rare:144 | ||||
| chr12:53251897-53252277 | Common:10; Rare:337 | ||||
| chr12:53252540-53252950 | Common:7; Rare:225 | ||||
| chr12:53268263-53268393 | Common:1; Rare:29 | ||||
| chr12:53295388-53295774 | Common:7; Rare:274 | ||||
| chr12:53299585-53299986 | Common:7; Rare:539 | ||||
| chr12:53305726-53307194 | Common:7; Rare:716 | ||||
| chr12:53321140-53321470 | Common:6; Rare:292; Clinvar:6; Clinvar (pathogenic):6 | ||||
| chr12:53321484-53321717 | Common:3; Rare:166; Clinvar:9 | ||||
| chr12:53324700-53325220 | Common:3; Rare:233 | ||||
| chr12:53344520-53345020 | Common:2; Rare:128 | ||||
| chr12:53345040-53345620 | Common:4; Rare:96 |