| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57604578-57604845 | Rare:46 | ||||
| chr12:57610051-57610196 | Common:2; Rare:27 | ||||
| chr12:57610239-57610315 | Common:1; Rare:36 | ||||
| chr12:57611191-57611481 | Rare:62 | ||||
| chr12:57694561-57694774 | Rare:39 | ||||
| chr12:57716403-57716743 | Rare:98 | ||||
| chr12:57744822-57745096 | Common:1; Rare:58 | ||||
| chr12:57745288-57745429 | Common:1; Rare:20 | ||||
| chr12:57752248-57752421 | Rare:46; Clinvar:1 | ||||
| chr12:57766115-57766265 | Rare:54; Clinvar (pathogenic):1 | ||||
| chr12:57772068-57772244 | Rare:68 | ||||
| chr12:57772520-57772670 | Common:3; Rare:22 | ||||
| chr12:57846376-57846483 | Rare:36 | ||||
| chr12:57846903-57847221 | Common:2; Rare:114 | ||||
| chr12:57941360-57941704 | Common:3; Rare:102 |