Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10815308-10815434 | Rare:21 | ||||
chr1:11069711-11069930 | Common:1; Rare:45 | ||||
chr1:11070958-11071255 | Common:1; Rare:71 | ||||
chr1:11087823-11088126 | Common:3; Rare:86 | ||||
chr1:11676062-11676371 | Common:3; Rare:67 | ||||
chr1:11790872-11791196 | Common:6; Rare:94; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:12414994-12415201 | Rare:49 | ||||
chr1:12612579-12612777 | Common:1; Rare:32 | ||||
chr1:12614838-12615035 | Common:1; Rare:34 | ||||
chr1:12619095-12619236 | Rare:32 | ||||
chr1:14304395-14304630 | Common:1; Rare:42 | ||||
chr1:15603561-15603719 | Common:3; Rare:49 | ||||
chr1:15834661-15835133 | Common:2; Rare:201 | ||||
chr1:15835793-15836134 | Common:6; Rare:165 | ||||
chr1:15948475-15948774 | Common:2; Rare:61 |