Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:9102469-9102796 | Common:2; Rare:137; Clinvar:6; Clinvar (benign):2 | ||||
chr18:9136529-9136903 | Rare:139 | ||||
chr18:9708055-9708339 | Common:4; Rare:70 | ||||
chr18:9914158-9914331 | Rare:67 | ||||
chr18:11851246-11851625 | Common:3; Rare:142 | ||||
chr18:11851627-11851791 | Rare:50 | ||||
chr18:11851794-11852406 | Common:4; Rare:185 | ||||
chr18:11908236-11908428 | Rare:57 | ||||
chr18:11980810-11981031 | Common:4; Rare:73 | ||||
chr18:12702627-12703137 | Common:3; Rare:199 | ||||
chr18:12884161-12884425 | Common:4; Rare:129 | ||||
chr18:12991182-12991410 | Common:2; Rare:81 | ||||
chr18:13726462-13726724 | Common:3; Rare:102 | ||||
chr18:21600620-21600774 | Rare:43 | ||||
chr18:23503287-23503542 | Common:2; Rare:89 |