| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76084593-76085250 | Common:11; Rare:209 | ||||
| chr12:76348290-76348610 | Common:3; Rare:163; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:76559489-76559998 | Common:2; Rare:268 | ||||
| chr12:76763948-76764285 | Common:5; Rare:237 | ||||
| chr12:76878854-76879216 | Rare:180 | ||||
| chr12:77065453-77065803 | Common:2; Rare:196 | ||||
| chr12:78863680-78864047 | Common:3; Rare:101 | ||||
| chr12:79689180-79689660 | Common:4; Rare:172 | ||||
| chr12:79690290-79690729 | Common:4; Rare:208 | ||||
| chr12:79690884-79691258 | Common:2; Rare:245 | ||||
| chr12:79934900-79935430 | Common:2; Rare:381 | ||||
| chr12:82358342-82358566 | Rare:195 | ||||
| chr12:82358743-82358908 | Common:6; Rare:150 | ||||
| chr12:82686620-82687170 | Common:3; Rare:237 | ||||
| chr12:84912529-84912918 | Common:2; Rare:145 |