| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:16332762-16333007 | Rare:118 | ||||
| chr12:16348990-16349400 | Common:6; Rare:165 | ||||
| chr12:16352452-16352852 | Common:3; Rare:75 | ||||
| chr12:16531629-16531819 | Rare:33 | ||||
| chr12:17601023-17601594 | Common:10; Rare:299 | ||||
| chr12:17995495-17995895 | Common:2; Rare:113 | ||||
| chr12:18502354-18502866 | Common:2; Rare:201 | ||||
| chr12:18676163-18676563 | Common:2; Rare:87 | ||||
| chr12:19431537-19432351 | Common:4; Rare:256 | ||||
| chr12:19689841-19690241 | Common:6; Rare:148 | ||||
| chr12:19775388-19775521 | Common:1; Rare:30 | ||||
| chr12:20963520-20964170 | Common:3; Rare:119 | ||||
| chr12:21471394-21472232 | Common:12; Rare:319; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:21675050-21675440 | Common:2; Rare:77 | ||||
| chr12:21725821-21727331 | Common:21; Rare:563 |