Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:12947666-12948092 | Common:3; Rare:123 | ||||
chr18:12991194-12991390 | Common:1; Rare:69 | ||||
chr18:13726443-13726720 | Common:3; Rare:109 | ||||
chr18:21111668-21111938 | Common:2; Rare:93 | ||||
chr18:21600650-21600856 | Rare:49 | ||||
chr18:23453177-23453345 | Rare:58 | ||||
chr18:23586387-23586533 | Common:2; Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
chr18:24397801-24397992 | Common:2; Rare:80 | ||||
chr18:25352072-25352410 | Common:2; Rare:135 | ||||
chr18:31162895-31163214 | Common:2; Rare:56 | ||||
chr18:31498050-31498259 | Common:1; Rare:65; Clinvar:4; Clinvar (benign):5 | ||||
chr18:31943098-31943375 | Common:7; Rare:89 | ||||
chr18:32092368-32092727 | Common:5; Rare:165 | ||||
chr18:35240912-35241090 | Common:2; Rare:67 | ||||
chr18:35290193-35290377 | Common:2; Rare:67 |