| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:23949651-23949874 | Common:4; Rare:34 | ||||
| chr12:25195119-25195299 | Common:2; Rare:50 | ||||
| chr12:26937961-26938186 | Common:8; Rare:65 | ||||
| chr12:26938282-26938534 | Common:3; Rare:96 | ||||
| chr12:27523990-27524158 | Rare:42 | ||||
| chr12:28190360-28190481 | Common:1; Rare:36 | ||||
| chr12:30754947-30755013 | Rare:24 | ||||
| chr12:31073769-31073892 | Rare:50 | ||||
| chr12:31729015-31729265 | Rare:74 | ||||
| chr12:31959293-31959449 | Common:2; Rare:51 | ||||
| chr12:32896767-32896974 | Common:1; Rare:67; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:38905580-38905748 | Common:3; Rare:45 | ||||
| chr12:42326065-42326206 | Common:1; Rare:43 | ||||
| chr12:43758745-43758941 | Rare:47 | ||||
| chr12:43806272-43806415 | Common:2; Rare:45 |