| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46273746-46274331 | Common:3; Rare:205 | ||||
| chr18:46332980-46333300 | Common:1; Rare:60 | ||||
| chr18:46424940-46425330 | Common:3; Rare:87 | ||||
| chr18:46465990-46466680 | Common:6; Rare:113 | ||||
| chr18:46468360-46468800 | Common:2; Rare:70 | ||||
| chr18:46469486-46469864 | Rare:57 | ||||
| chr18:46528962-46529578 | Common:12; Rare:300; Clinvar:11; Clinvar (benign):14; Clinvar (pathogenic):5 | ||||
| chr18:46868223-46868462 | Rare:40 | ||||
| chr18:47595730-47596090 | Common:2; Rare:55 | ||||
| chr18:48002974-48003396 | Common:9; Rare:195 | ||||
| chr18:48008190-48008650 | Common:7; Rare:271 | ||||
| chr18:48054100-48054505 | Common:10; Rare:235 | ||||
| chr18:48106937-48107806 | Common:26; Rare:363 | ||||
| chr18:48139330-48140150 | Common:7; Rare:240 | ||||
| chr18:48142380-48142880 | Common:7; Rare:82 |