| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:5431929-5432322 | Common:6; Rare:134 | ||||
| chr12:5432519-5432750 | Common:8; Rare:45 | ||||
| chr12:5432910-5433037 | Rare:35 | ||||
| chr12:6341912-6342166 | Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6383985-6384272 | Common:1; Rare:63 | ||||
| chr12:6451809-6452149 | Common:4; Rare:66 | ||||
| chr12:6493219-6493394 | Common:6; Rare:48 | ||||
| chr12:6493746-6494140 | Common:2; Rare:116 | ||||
| chr12:6533491-6533620 | Rare:28 | ||||
| chr12:6534225-6534882 | Common:9; Rare:258 | ||||
| chr12:6535820-6536144 | Common:2; Rare:86 | ||||
| chr12:6536344-6536504 | Common:1; Rare:55 | ||||
| chr12:6536529-6536745 | Rare:78 | ||||
| chr12:6548790-6549026 | Common:1; Rare:74 | ||||
| chr12:6549061-6549280 | Common:1; Rare:44 |