| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57771718-57772012 | Rare:64 | ||||
| chr12:57772044-57772305 | Rare:89 | ||||
| chr12:57772482-57772634 | Common:2; Rare:30 | ||||
| chr12:57772646-57772890 | Common:3; Rare:68 | ||||
| chr12:57772942-57773031 | Rare:32 | ||||
| chr12:57782643-57782861 | Common:2; Rare:83; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:57845516-57845726 | Common:2; Rare:57 | ||||
| chr12:57845745-57845881 | Common:2; Rare:34 | ||||
| chr12:57846063-57846225 | Rare:43 | ||||
| chr12:57846388-57846510 | Rare:41 | ||||
| chr12:57846659-57846816 | Common:1; Rare:55 | ||||
| chr12:57846873-57847287 | Common:5; Rare:151 | ||||
| chr12:57941205-57941623 | Common:5; Rare:123 | ||||
| chr12:57941635-57941743 | Rare:33 | ||||
| chr12:57941746-57941859 | Common:1; Rare:36 |