| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:83014585-83014783 | Common:5; Rare:36 | ||||
| chr12:85826572-85826657 | Common:9; Rare:18 | ||||
| chr12:85834243-85834327 | Common:2; Rare:14 | ||||
| chr12:85903490-85903613 | Rare:14 | ||||
| chr12:87111545-87111621 | Rare:11 | ||||
| chr12:87951861-87951985 | Common:1; Rare:20 | ||||
| chr12:88042288-88042492 | Common:1; Rare:41 | ||||
| chr12:88068513-88068532 | Rare:9; Clinvar (benign):1 | ||||
| chr12:88130335-88130563 | Rare:61; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:88130950-88131214 | Rare:46; Clinvar (pathogenic):1 | ||||
| chr12:88138852-88139162 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:88139496-88139708 | Rare:64; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:88170034-88170334 | Common:1; Rare:47 | ||||
| chr12:88299912-88300050 | Common:1; Rare:26 | ||||
| chr12:88563694-88563934 | Common:1; Rare:43 |