| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:58578568-58578627 | Rare:8 | ||||
| chr18:58578955-58579078 | Rare:36 | ||||
| chr18:58579530-58579855 | Common:1; Rare:109 | ||||
| chr18:58671062-58671084 | Common:1; Rare:10 | ||||
| chr18:58671088-58671647 | Common:4; Rare:217; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:58671731-58671813 | Rare:14 | ||||
| chr18:58862858-58862970 | Rare:18 | ||||
| chr18:58863122-58863719 | Common:11; Rare:165 | ||||
| chr18:58864054-58864131 | Common:1; Rare:28 | ||||
| chr18:58864386-58864541 | Rare:32 | ||||
| chr18:58864738-58864937 | Rare:42 | ||||
| chr18:59139464-59139536 | Rare:14 | ||||
| chr18:59139620-59139956 | Common:3; Rare:86 | ||||
| chr18:59140078-59140114 | Common:1; Rare:8 | ||||
| chr18:59140124-59140415 | Common:2; Rare:52 |