| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:54958065-54958152 | Rare:16 | ||||
| chr18:54959352-54959509 | Common:1; Rare:42 | ||||
| chr18:55586056-55586190 | Common:1; Rare:47 | ||||
| chr18:55588061-55588144 | Rare:23; Clinvar (benign):1 | ||||
| chr18:55589686-55589923 | Common:1; Rare:67 | ||||
| chr18:55635924-55636063 | Rare:22 | ||||
| chr18:55665159-55665277 | Common:1; Rare:25 | ||||
| chr18:56651119-56651729 | Common:9; Rare:154 | ||||
| chr18:56721363-56721541 | Common:1; Rare:25 | ||||
| chr18:57147012-57147649 | Common:6; Rare:196 | ||||
| chr18:57586595-57586811 | Rare:60 | ||||
| chr18:57621707-57621964 | Common:3; Rare:91 | ||||
| chr18:58195699-58195745 | Rare:17 | ||||
| chr18:58862680-58862963 | Common:1; Rare:51 | ||||
| chr18:58864766-58864902 | Rare:29 |