Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23801506-23801658 | Rare:31 | ||||
chr1:23865517-23865767 | Common:2; Rare:63; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:23904837-23905045 | Common:1; Rare:30 | ||||
chr1:23930921-23931259 | Common:2; Rare:59 | ||||
chr1:23931337-23931424 | Common:1; Rare:9 | ||||
chr1:23955234-23955406 | Common:1; Rare:18 | ||||
chr1:23965007-23965035 | Rare:1 | ||||
chr1:24018836-24019170 | Common:2; Rare:50 | ||||
chr1:24022743-24023006 | Common:1; Rare:38 | ||||
chr1:24119963-24119981 | Rare:1 | ||||
chr1:24120148-24120257 | Rare:28 | ||||
chr1:24120404-24120561 | Rare:22 | ||||
chr1:24149877-24150135 | Common:1; Rare:51 | ||||
chr1:24150568-24150810 | Common:1; Rare:45 | ||||
chr1:24151245-24151524 | Common:2; Rare:53 |