| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56645887-56646292 | Common:1; Rare:110 | ||||
| chr12:56687993-56688579 | Common:5; Rare:210 | ||||
| chr12:56712784-56713139 | Common:2; Rare:74 | ||||
| chr12:56724941-56725554 | Common:3; Rare:159 | ||||
| chr12:56752310-56752515 | Rare:58 | ||||
| chr12:57087831-57088061 | Common:1; Rare:63 | ||||
| chr12:57229966-57230194 | Rare:50 | ||||
| chr12:57430735-57431089 | Common:1; Rare:93 | ||||
| chr12:57488796-57489099 | Common:3; Rare:71; Clinvar (benign):2 | ||||
| chr12:57512695-57512772 | Rare:17; Clinvar (benign):1 | ||||
| chr12:57514793-57515331 | Common:3; Rare:171; Clinvar:5; Clinvar (benign):7 | ||||
| chr12:57520417-57520720 | Common:2; Rare:86 | ||||
| chr12:57694233-57694319 | Common:1; Rare:16 | ||||
| chr12:57720196-57720517 | Rare:99 | ||||
| chr12:57744822-57745175 | Common:2; Rare:83 |