| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134275375-134275583 | Common:5; Rare:42 | ||||
| chr11:134276059-134276085 | Rare:6 | ||||
| chr11:134488764-134488891 | Common:1; Rare:18 | ||||
| chr11:134712347-134712458 | Common:3; Rare:43 | ||||
| chr12:16747-16843 | Common:4; Rare:31 | ||||
| chr12:92361-92529 | Common:2; Rare:27 | ||||
| chr12:192764-193002 | Common:4; Rare:67 | ||||
| chr12:547072-547233 | Common:2; Rare:35 | ||||
| chr12:585458-585566 | Common:6; Rare:21 | ||||
| chr12:698240-698383 | Common:1; Rare:25 | ||||
| chr12:753773-754003 | Common:3; Rare:82; Clinvar:7; Clinvar (benign):4 | ||||
| chr12:1173950-1174146 | Common:1; Rare:40 | ||||
| chr12:1650340-1650518 | Rare:25 | ||||
| chr12:1907652-1907894 | Common:3; Rare:66; Clinvar:1 | ||||
| chr12:1922089-1922180 | Rare:33 |