| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:54959364-54959511 | Common:1; Rare:38 | ||||
| chr18:55589744-55589996 | Common:2; Rare:83 | ||||
| chr18:56651133-56651413 | Common:4; Rare:74 | ||||
| chr18:57586595-57586813 | Rare:61 | ||||
| chr18:57621713-57621997 | Common:3; Rare:102 | ||||
| chr18:58864786-58864888 | Rare:19 | ||||
| chr18:59697643-59697860 | Common:1; Rare:57 | ||||
| chr18:62186938-62187329 | Common:5; Rare:108 | ||||
| chr18:63422370-63422696 | Common:2; Rare:94 | ||||
| chr18:63970000-63970134 | Rare:25 | ||||
| chr18:68714987-68715260 | Common:5; Rare:123 | ||||
| chr18:70205659-70205743 | Common:2; Rare:42; Clinvar (benign):2 | ||||
| chr18:74148320-74148546 | Common:2; Rare:82 | ||||
| chr18:74291906-74292276 | Common:4; Rare:111 | ||||
| chr18:74496029-74496401 | Common:4; Rare:117 |