| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:712518-712810 | Common:3; Rare:122 | ||||
| chr18:812209-812421 | Common:1; Rare:75 | ||||
| chr18:812531-812603 | Common:1; Rare:16 | ||||
| chr18:812741-812923 | Rare:50 | ||||
| chr18:2571442-2571593 | Rare:51 | ||||
| chr18:2655843-2656183 | Common:4; Rare:109; Clinvar:5; Clinvar (benign):1 | ||||
| chr18:3247332-3247908 | Common:1; Rare:166 | ||||
| chr18:3261792-3262236 | Common:6; Rare:143 | ||||
| chr18:3449087-3449337 | Common:5; Rare:62 | ||||
| chr18:3449936-3450216 | Common:1; Rare:80 | ||||
| chr18:6729858-6729923 | Rare:20 | ||||
| chr18:7117733-7117931 | Common:4; Rare:64 | ||||
| chr18:9102483-9102766 | Common:2; Rare:112; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136442-9137047 | Rare:212 | ||||
| chr18:9334472-9334867 | Common:1; Rare:97 |