| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:25075472-25075741 | Common:10; Rare:55 | ||||
| chr12:25195155-25195393 | Common:1; Rare:69 | ||||
| chr12:25250406-25250564 | Common:1; Rare:47 | ||||
| chr12:25250806-25251060 | Rare:89; Clinvar:5; Clinvar (benign):4 | ||||
| chr12:25251196-25251361 | Rare:37 | ||||
| chr12:26122508-26122546 | Rare:10 | ||||
| chr12:26125014-26125206 | Common:1; Rare:45 | ||||
| chr12:26125218-26125520 | Common:3; Rare:56 | ||||
| chr12:26832350-26832545 | Common:1; Rare:43 | ||||
| chr12:26832889-26832967 | Common:2; Rare:15 | ||||
| chr12:26833014-26833560 | Common:3; Rare:141 | ||||
| chr12:26937865-26938183 | Common:8; Rare:82 | ||||
| chr12:26938225-26938790 | Common:4; Rare:206 | ||||
| chr12:27013407-27013704 | Common:1; Rare:43 | ||||
| chr12:27014174-27014655 | Common:1; Rare:144 |