| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:4887706-4887740 | Rare:2 | ||||
| chr9:5080109-5080352 | Rare:63; Clinvar:2 | ||||
| chr9:5630084-5630222 | Common:1; Rare:38 | ||||
| chr9:5768700-5769046 | Common:2; Rare:108 | ||||
| chr9:5898279-5898367 | Rare:20 | ||||
| chr9:5926193-5926489 | Common:1; Rare:78 | ||||
| chr9:15468961-15469281 | Common:2; Rare:102 | ||||
| chr9:15469301-15469399 | Common:1; Rare:32 | ||||
| chr9:15486011-15486140 | Rare:45 | ||||
| chr9:15486827-15487114 | Common:3; Rare:77 | ||||
| chr9:19378366-19378930 | Common:1; Rare:166 | ||||
| chr9:33445347-33445512 | Common:1; Rare:25 | ||||
| chr9:33446355-33446454 | Rare:20 | ||||
| chr9:33818743-33818949 | Rare:43 | ||||
| chr9:33916705-33917054 | Common:1; Rare:80 |