| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74597573-74597929 | Common:2; Rare:97 | ||||
| chr18:75208969-75209260 | Common:2; Rare:113 | ||||
| chr18:76495201-76495529 | Common:2; Rare:89 | ||||
| chr18:76822215-76822636 | Common:11; Rare:119 | ||||
| chr18:77087436-77087526 | Common:4; Rare:29 | ||||
| chr18:77087549-77087616 | Common:1; Rare:15 | ||||
| chr18:77132584-77132919 | Common:3; Rare:97 | ||||
| chr18:79400228-79400338 | Common:2; Rare:41 | ||||
| chr18:79964562-79964742 | Common:2; Rare:52 | ||||
| chr18:79970359-79970552 | Common:1; Rare:60 | ||||
| chr18:79988294-79988661 | Common:4; Rare:123; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr18:80034174-80034521 | Common:5; Rare:134 | ||||
| chr19:344786-344945 | Common:3; Rare:55 | ||||
| chr19:572339-572701 | Common:1; Rare:185 | ||||
| chr19:633462-633745 | Common:8; Rare:131 |