| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:58920440-58920800 | Common:4; Rare:173 | ||||
| chr12:59595862-59596214 | Common:5; Rare:78 | ||||
| chr12:59596960-59597180 | Common:2; Rare:95 | ||||
| chr12:62259764-62260129 | Rare:102 | ||||
| chr12:62260133-62260496 | Common:1; Rare:222 | ||||
| chr12:62466626-62466894 | Rare:145 | ||||
| chr12:62467100-62467570 | Common:2; Rare:154 | ||||
| chr12:63779764-63779919 | Common:4; Rare:105; Clinvar (benign):1 | ||||
| chr12:63843621-63844264 | Common:10; Rare:194 | ||||
| chr12:63844570-63844860 | Common:1; Rare:114 | ||||
| chr12:64222223-64222350 | Rare:86 | ||||
| chr12:64404198-64404639 | Common:10; Rare:309 | ||||
| chr12:64404971-64405159 | Rare:63 | ||||
| chr12:64451999-64452340 | Common:2; Rare:176 | ||||
| chr12:64610156-64610545 | Common:11; Rare:223 |