| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:55586098-55586166 | Rare:26 | ||||
| chr18:55589680-55589979 | Common:2; Rare:94 | ||||
| chr18:56651129-56651413 | Common:4; Rare:74 | ||||
| chr18:56651610-56651714 | Common:3; Rare:25 | ||||
| chr18:58045545-58045745 | Rare:56 | ||||
| chr18:58864825-58864912 | Rare:15 | ||||
| chr18:59359241-59359564 | Common:3; Rare:142; Clinvar:1 | ||||
| chr18:62186937-62187334 | Common:5; Rare:108 | ||||
| chr18:63367124-63367369 | Common:1; Rare:91 | ||||
| chr18:63422364-63422716 | Common:2; Rare:103 | ||||
| chr18:63969941-63970154 | Common:6; Rare:42 | ||||
| chr18:65750744-65751070 | Common:2; Rare:104 | ||||
| chr18:68714977-68715296 | Common:7; Rare:135 | ||||
| chr18:70205654-70205774 | Common:3; Rare:49; Clinvar (benign):2 | ||||
| chr18:74148352-74148587 | Common:1; Rare:72 |