| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12356981-12357196 | Common:4; Rare:111 | ||||
| chr12:12561096-12561279 | Common:1; Rare:37 | ||||
| chr12:12562513-12562866 | Rare:96 | ||||
| chr12:12611627-12612186 | Common:3; Rare:164 | ||||
| chr12:12696646-12696744 | Rare:33 | ||||
| chr12:12717234-12717502 | Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12717597-12717646 | Rare:15; Clinvar (benign):1 | ||||
| chr12:12891364-12891617 | Common:1; Rare:47 | ||||
| chr12:13000035-13000476 | Common:2; Rare:138 | ||||
| chr12:14365492-14365719 | Common:1; Rare:74 | ||||
| chr12:14567677-14567751 | Common:1; Rare:26 | ||||
| chr12:14770020-14770092 | Rare:13 | ||||
| chr12:14771087-14771149 | Common:1; Rare:41 | ||||
| chr12:14774184-14774668 | Common:3; Rare:155 | ||||
| chr12:14774821-14774850 | Rare:10 |