| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55927768-55928097 | Rare:95 | ||||
| chr12:55966653-55966907 | Rare:124 | ||||
| chr12:55973955-55974245 | Common:2; Rare:77 | ||||
| chr12:55974408-55974554 | Rare:30 | ||||
| chr12:55997113-55997347 | Common:2; Rare:128; Clinvar:4 | ||||
| chr12:56007130-56007640 | Common:2; Rare:148 | ||||
| chr12:56007610-56008030 | Common:2; Rare:103 | ||||
| chr12:56041484-56042325 | Common:18; Rare:557; Clinvar:6; Clinvar (benign):13 | ||||
| chr12:56079790-56080205 | Common:8; Rare:145 | ||||
| chr12:56104177-56104811 | Common:10; Rare:404 | ||||
| chr12:56116482-56116875 | Common:4; Rare:142 | ||||
| chr12:56116920-56117360 | Common:4; Rare:156 | ||||
| chr12:56117962-56118319 | Common:1; Rare:221 | ||||
| chr12:56127853-56128345 | Rare:178 | ||||
| chr12:56152419-56152646 | Rare:132 |