| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2004408-2004626 | Common:1; Rare:85 | ||||
| chr12:2812886-2813057 | Rare:46 | ||||
| chr12:2876926-2877271 | Common:1; Rare:105 | ||||
| chr12:2890593-2890950 | Common:1; Rare:149 | ||||
| chr12:3873337-3873512 | Common:1; Rare:40 | ||||
| chr12:4273609-4273843 | Rare:68 | ||||
| chr12:4275455-4275703 | Common:3; Rare:45 | ||||
| chr12:4320949-4321284 | Common:5; Rare:131 | ||||
| chr12:4538436-4538930 | Common:3; Rare:112 | ||||
| chr12:4648994-4649154 | Common:2; Rare:54; Clinvar (benign):1 | ||||
| chr12:6200042-6200348 | Common:3; Rare:79 | ||||
| chr12:6451813-6452132 | Common:4; Rare:61 | ||||
| chr12:6493175-6493502 | Common:8; Rare:99 | ||||
| chr12:6493778-6494138 | Common:2; Rare:108 | ||||
| chr12:6534355-6534578 | Common:5; Rare:95 |