| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:31465270-31465353 | Common:1; Rare:19 | ||||
| chr18:31487703-31487942 | Common:2; Rare:50 | ||||
| chr18:31513602-31513720 | Common:1; Rare:24 | ||||
| chr18:31520936-31521242 | Common:1; Rare:77; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr18:31524443-31524723 | Common:1; Rare:72; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):4 | ||||
| chr18:31861947-31862129 | Common:1; Rare:24 | ||||
| chr18:31911845-31911875 | Rare:10 | ||||
| chr18:32136065-32136305 | Rare:41 | ||||
| chr18:35306246-35306280 | Rare:6 | ||||
| chr18:35473046-35473176 | Common:1; Rare:19 | ||||
| chr18:35477616-35477891 | Common:2; Rare:38 | ||||
| chr18:35478265-35478873 | Common:3; Rare:108 | ||||
| chr18:35994936-35995048 | Rare:20 | ||||
| chr18:36755431-36755462 | Common:1; Rare:4 | ||||
| chr18:37558404-37558572 | Common:1; Rare:29 |