| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:49490452-49490914 | Common:1; Rare:114 | ||||
| chr18:49561879-49562153 | Rare:66 | ||||
| chr18:49813812-49814110 | Common:1; Rare:122 | ||||
| chr18:50879015-50879228 | Common:4; Rare:73 | ||||
| chr18:54269443-54269629 | Common:2; Rare:89 | ||||
| chr18:55321707-55321909 | Rare:45 | ||||
| chr18:55322361-55322548 | Rare:39 | ||||
| chr18:55401645-55401814 | Rare:33 | ||||
| chr18:55589707-55590005 | Common:2; Rare:98 | ||||
| chr18:56651129-56651394 | Common:4; Rare:66 | ||||
| chr18:57586596-57586987 | Common:1; Rare:90; Clinvar (benign):1 | ||||
| chr18:57621710-57621969 | Common:3; Rare:93 | ||||
| chr18:59697642-59697852 | Common:1; Rare:58 | ||||
| chr18:59899818-59900027 | Common:3; Rare:70 | ||||
| chr18:62186929-62187328 | Common:5; Rare:110 |