| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57205154-57205448 | Rare:99 | ||||
| chr12:57211947-57212132 | Common:1; Rare:46 | ||||
| chr12:57462744-57462899 | Common:1; Rare:35 | ||||
| chr12:57490270-57490564 | Rare:66; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:57893901-57894211 | Rare:40 | ||||
| chr12:57936061-57936242 | Common:2; Rare:49 | ||||
| chr12:59105032-59105230 | Common:4; Rare:46 | ||||
| chr12:59323604-59323813 | Common:3; Rare:54 | ||||
| chr12:59324227-59324323 | Common:1; Rare:25 | ||||
| chr12:59325817-59325964 | Common:2; Rare:30 | ||||
| chr12:59327741-59327795 | Rare:15 | ||||
| chr12:59327886-59327913 | Common:1; Rare:6 | ||||
| chr12:59328608-59328709 | Common:2; Rare:33 | ||||
| chr12:62602744-62602882 | Common:1; Rare:60 | ||||
| chr12:63823966-63824080 | Common:2; Rare:16 |