| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:14748070-14748416 | Common:5; Rare:107 | ||||
| chr18:21111576-21111941 | Common:2; Rare:118 | ||||
| chr18:21600644-21600778 | Rare:37 | ||||
| chr18:22169508-22169589 | Rare:25 | ||||
| chr18:22933285-22933402 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:23453115-23453336 | Rare:80 | ||||
| chr18:23503340-23503542 | Rare:73 | ||||
| chr18:23884361-23884685 | Common:1; Rare:58 | ||||
| chr18:24271235-24271349 | Common:2; Rare:13 | ||||
| chr18:24397758-24398073 | Common:2; Rare:115 | ||||
| chr18:25352018-25352406 | Common:2; Rare:150 | ||||
| chr18:31943098-31943376 | Common:7; Rare:90 | ||||
| chr18:32092416-32092748 | Common:4; Rare:151 | ||||
| chr18:34493211-34493369 | Common:1; Rare:42 | ||||
| chr18:35240917-35241100 | Common:2; Rare:69 |