| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:66130721-66130806 | Rare:28 | ||||
| chr12:68332265-68332631 | Common:1; Rare:123 | ||||
| chr12:68610695-68611050 | Common:1; Rare:148 | ||||
| chr12:68686816-68687062 | Common:4; Rare:76 | ||||
| chr12:68807968-68808259 | Common:3; Rare:94 | ||||
| chr12:68808858-68809037 | Rare:35 | ||||
| chr12:69470305-69470439 | Common:2; Rare:46 | ||||
| chr12:71663769-71664131 | Common:1; Rare:98 | ||||
| chr12:71839573-71839800 | Common:2; Rare:80 | ||||
| chr12:75390886-75391102 | Common:1; Rare:64 | ||||
| chr12:75480555-75480986 | Rare:91 | ||||
| chr12:75481654-75481851 | Common:2; Rare:44 | ||||
| chr12:76348360-76348545 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76763958-76764269 | Common:3; Rare:130 | ||||
| chr12:76878948-76879158 | Rare:73 |