| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:28190360-28190483 | Common:1; Rare:37 | ||||
| chr12:31073743-31073907 | Common:8; Rare:61 | ||||
| chr12:31324092-31324261 | Rare:41 | ||||
| chr12:31729015-31729270 | Rare:76 | ||||
| chr12:31959325-31959483 | Common:1; Rare:50 | ||||
| chr12:32502034-32502218 | Common:2; Rare:33; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:32679159-32679331 | Rare:69; Clinvar (benign):1 | ||||
| chr12:38905580-38905804 | Common:5; Rare:64 | ||||
| chr12:42326021-42326223 | Common:1; Rare:66 | ||||
| chr12:43758749-43759000 | Common:2; Rare:69; Clinvar:2 | ||||
| chr12:43806222-43806425 | Common:2; Rare:68 | ||||
| chr12:45216011-45216154 | Rare:44 | ||||
| chr12:45990491-45990895 | Common:2; Rare:127 | ||||
| chr12:46267842-46267974 | Common:1; Rare:25 | ||||
| chr12:46268616-46268833 | Common:1; Rare:59 |