| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:47150452-47150834 | Common:3; Rare:115 | ||||
| chr18:49487192-49487415 | Common:3; Rare:90 | ||||
| chr18:49813826-49814138 | Common:1; Rare:130 | ||||
| chr18:54224023-54224211 | Rare:56 | ||||
| chr18:54269317-54269622 | Common:2; Rare:121 | ||||
| chr18:55321647-55321948 | Rare:67 | ||||
| chr18:55423597-55423842 | Common:2; Rare:49 | ||||
| chr18:55510733-55511128 | Common:1; Rare:83 | ||||
| chr18:56651124-56651343 | Common:3; Rare:51 | ||||
| chr18:58221371-58221571 | Common:1; Rare:38 | ||||
| chr18:58671515-58671625 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:58864807-58864885 | Rare:15 | ||||
| chr18:58964013-58964136 | Rare:18 | ||||
| chr18:58964615-58964704 | Rare:19 | ||||
| chr18:59899718-59900044 | Common:3; Rare:108 |