| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2959843-2959907 | Common:1; Rare:14 | ||||
| chr12:3077267-3077453 | Common:6; Rare:79 | ||||
| chr12:3753053-3753358 | Common:2; Rare:68 | ||||
| chr12:4320949-4321258 | Common:5; Rare:117 | ||||
| chr12:4538444-4538940 | Common:3; Rare:112 | ||||
| chr12:4649045-4649149 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr12:6124371-6124764 | Rare:62; Clinvar:2 | ||||
| chr12:6124893-6124942 | Rare:16 | ||||
| chr12:6200004-6200485 | Common:4; Rare:138 | ||||
| chr12:6384005-6384250 | Common:1; Rare:51 | ||||
| chr12:6452038-6452125 | Common:1; Rare:20 | ||||
| chr12:6493175-6493502 | Common:8; Rare:99 | ||||
| chr12:6493752-6494140 | Common:2; Rare:114 | ||||
| chr12:6534296-6534582 | Common:5; Rare:121 | ||||
| chr12:6535170-6535414 | Common:2; Rare:75 |