| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12901141-12901289 | Rare:25 | ||||
| chr12:13098824-13098894 | Common:1; Rare:10 | ||||
| chr12:13101114-13101453 | Common:3; Rare:72 | ||||
| chr12:13197447-13197751 | Common:3; Rare:65 | ||||
| chr12:13197828-13198048 | Common:2; Rare:32 | ||||
| chr12:13198976-13199088 | Common:1; Rare:19 | ||||
| chr12:13201677-13201844 | Rare:36 | ||||
| chr12:13203064-13203364 | Common:1; Rare:71 | ||||
| chr12:13204589-13204663 | Common:1; Rare:16 | ||||
| chr12:13210070-13210324 | Common:1; Rare:50 | ||||
| chr12:13223196-13223353 | Rare:17 | ||||
| chr12:15688490-15688542 | Rare:9 | ||||
| chr12:16349088-16349439 | Common:2; Rare:69 | ||||
| chr12:16555904-16555980 | Rare:13 | ||||
| chr12:21852215-21852471 | Common:3; Rare:68; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 |