| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12350083-12350720 | Common:10; Rare:621 | ||||
| chr12:12356863-12357327 | Common:35; Rare:944 | ||||
| chr12:12357457-12357857 | Rare:151 | ||||
| chr12:12357854-12358398 | Common:5; Rare:182 | ||||
| chr12:12506028-12506595 | Common:3; Rare:138 | ||||
| chr12:12561015-12561415 | Common:3; Rare:131 | ||||
| chr12:12561466-12562502 | Common:6; Rare:545 | ||||
| chr12:12562530-12563038 | Common:2; Rare:322 | ||||
| chr12:12611550-12612310 | Common:17; Rare:625 | ||||
| chr12:12696023-12696470 | Common:8; Rare:397 | ||||
| chr12:12696601-12696856 | Rare:87 | ||||
| chr12:12714666-12714807 | Rare:65 | ||||
| chr12:12714791-12715191 | Common:4; Rare:95 | ||||
| chr12:12715247-12715647 | Common:6; Rare:134 | ||||
| chr12:12716703-12717621 | Common:10; Rare:954; Clinvar:9; Clinvar (benign):7 |