| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58466814-58467194 | Common:2; Rare:115 | ||||
| chr19:58475901-58476551 | Common:5; Rare:229 | ||||
| chr19:58499176-58499709 | Common:3; Rare:187; Clinvar:9; Clinvar (benign):2 | ||||
| chr19:58519455-58520143 | Common:1; Rare:171 | ||||
| chr19:58543917-58544519 | Common:5; Rare:235 | ||||
| chr19:58544619-58544766 | Rare:68 | ||||
| chr19:58554894-58555462 | Common:3; Rare:176 | ||||
| chr19:58557535-58557810 | Common:3; Rare:50 | ||||
| chr19:58558500-58558779 | Rare:85 | ||||
| chr19:58558821-58559264 | Common:3; Rare:139 | ||||
| chr19:58572658-58573068 | Common:2; Rare:120 | ||||
| chr19:58573262-58573520 | Rare:64 | ||||
| chr2:46500-46550 | Common:1; Rare:13 | ||||
| chr2:263657-263958 | Rare:63 | ||||
| chr2:264726-265037 | Common:2; Rare:159 |