Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23484170-23484490 | Common:2; Rare:97 | ||||
chr1:23484510-23484900 | Common:6; Rare:76 | ||||
chr1:23530868-23530995 | Rare:27 | ||||
chr1:23531207-23531471 | Common:2; Rare:37 | ||||
chr1:23558252-23558686 | Common:3; Rare:157 | ||||
chr1:23559434-23559696 | Common:2; Rare:111 | ||||
chr1:23691570-23691855 | Common:4; Rare:95; Clinvar:2; Clinvar (benign):2 | ||||
chr1:23692062-23693199 | Common:9; Rare:412; Clinvar:1; Clinvar (benign):4 | ||||
chr1:23743388-23743533 | Rare:52 | ||||
chr1:23778218-23778491 | Common:9; Rare:134 | ||||
chr1:23791060-23791222 | Rare:53 | ||||
chr1:23799485-23799838 | Common:1; Rare:63 | ||||
chr1:23800527-23800984 | Common:1; Rare:144 | ||||
chr1:23825342-23825609 | Common:3; Rare:82; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
chr1:23838579-23838735 | Common:1; Rare:26 |