| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144478279-144478369 | Rare:26 | ||||
| chr8:144509019-144509102 | Rare:25 | ||||
| chr8:144827247-144827608 | Common:1; Rare:95 | ||||
| chr8:145052142-145052478 | Common:11; Rare:82 | ||||
| chr9:4679444-4679616 | Rare:80 | ||||
| chr9:21031584-21031690 | Common:1; Rare:47 | ||||
| chr9:33025068-33025285 | Common:6; Rare:86 | ||||
| chr9:33264743-33265068 | Rare:85 | ||||
| chr9:34048877-34048992 | Common:1; Rare:46 | ||||
| chr9:35658016-35658354 | Common:6; Rare:233; Clinvar:16; Clinvar (benign):10; Clinvar (pathogenic):29 | ||||
| chr9:35689706-35689976 | Common:3; Rare:90; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35732078-35732356 | Common:2; Rare:83 | ||||
| chr9:35732365-35732683 | Common:3; Rare:81 | ||||
| chr9:36258446-36258578 | Common:2; Rare:27; Clinvar:1 | ||||
| chr9:37800707-37800837 | Rare:40 |