Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:238060738-238061057 | Common:4; Rare:99 | ||||
chr2:240025261-240025455 | Common:2; Rare:72; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:240560766-240560835 | Rare:29 | ||||
chr2:240561010-240561314 | Common:4; Rare:142 | ||||
chr2:241271945-241272110 | Common:1; Rare:38 | ||||
chr2:241315132-241315390 | Common:5; Rare:84 | ||||
chr2:241315656-241315982 | Common:5; Rare:129 | ||||
chr2:241637075-241637292 | Common:1; Rare:74 | ||||
chr2:241637534-241637704 | Common:1; Rare:92 | ||||
chr20:380722-381163 | Common:4; Rare:117 | ||||
chr20:381190-381349 | Common:2; Rare:40 | ||||
chr20:1118431-1118667 | Common:4; Rare:80 | ||||
chr20:1894436-1894498 | Rare:15 | ||||
chr20:1894827-1895127 | Rare:113 | ||||
chr20:2470737-2471083 | Common:4; Rare:108 |