Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:11908274-11908466 | Common:2; Rare:59 | ||||
chr18:11980924-11981031 | Common:2; Rare:31 | ||||
chr18:12702658-12703099 | Common:3; Rare:178 | ||||
chr18:12884134-12884425 | Common:4; Rare:149 | ||||
chr18:12947666-12948092 | Common:3; Rare:123 | ||||
chr18:12991125-12991417 | Common:2; Rare:109 | ||||
chr18:13726443-13726726 | Common:3; Rare:109 | ||||
chr18:21111572-21111923 | Common:2; Rare:113 | ||||
chr18:22169508-22169589 | Rare:25 | ||||
chr18:22933240-22933426 | Common:3; Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
chr18:22933764-22933889 | Common:1; Rare:50 | ||||
chr18:23453172-23453348 | Rare:61 | ||||
chr18:23503335-23503542 | Rare:75 | ||||
chr18:23586379-23586597 | Common:3; Rare:99; Clinvar:3; Clinvar (benign):2 | ||||
chr18:23884364-23884657 | Common:1; Rare:54 |