| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6452078-6452139 | Common:1; Rare:16 | ||||
| chr12:6493224-6493502 | Common:7; Rare:82 | ||||
| chr12:6493754-6494146 | Common:2; Rare:114 | ||||
| chr12:6534596-6534860 | Common:3; Rare:107 | ||||
| chr12:6535302-6535405 | Common:1; Rare:24 | ||||
| chr12:6568241-6568371 | Rare:50 | ||||
| chr12:6723936-6724142 | Common:1; Rare:50 | ||||
| chr12:6752967-6753213 | Common:6; Rare:81 | ||||
| chr12:6851890-6852174 | Rare:72 | ||||
| chr12:6867379-6867555 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6873334-6873541 | Common:1; Rare:55 | ||||
| chr12:6970616-6970976 | Common:4; Rare:115; Clinvar (benign):1 | ||||
| chr12:7018468-7018584 | Common:1; Rare:30 | ||||
| chr12:7108481-7108669 | Common:1; Rare:56 | ||||
| chr12:7130273-7130432 | Common:4; Rare:44 |