| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:9615047-9615153 | Common:1; Rare:26 | ||||
| chr18:9708040-9708354 | Common:5; Rare:78 | ||||
| chr18:9913771-9914280 | Common:1; Rare:191 | ||||
| chr18:10525803-10526161 | Common:2; Rare:126 | ||||
| chr18:10526271-10526515 | Common:2; Rare:89 | ||||
| chr18:11851167-11851487 | Common:3; Rare:116 | ||||
| chr18:11908240-11908657 | Common:3; Rare:113 | ||||
| chr18:11908813-11909054 | Common:2; Rare:73 | ||||
| chr18:11909672-11909725 | Rare:7 | ||||
| chr18:11980352-11980536 | Common:3; Rare:40 | ||||
| chr18:11980849-11981043 | Common:4; Rare:60 | ||||
| chr18:11981205-11981529 | Common:5; Rare:90 | ||||
| chr18:12307955-12308299 | Common:6; Rare:133 | ||||
| chr18:12376797-12377003 | Rare:77; Clinvar (benign):2 | ||||
| chr18:12377014-12377291 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):8 |