Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1159545-1159700 | Common:1; Rare:39 | ||||
chr1:1160578-1160819 | Common:3; Rare:46 | ||||
chr1:1162626-1162948 | Common:2; Rare:111 | ||||
chr1:1165291-1165595 | Common:2; Rare:61 | ||||
chr1:1166918-1167183 | Rare:78 | ||||
chr1:1705766-1706067 | Common:7; Rare:43 | ||||
chr1:1833432-1833696 | Common:1; Rare:59 | ||||
chr1:1892228-1892315 | Rare:18 | ||||
chr1:2047367-2047519 | Common:1; Rare:25 | ||||
chr1:2180246-2180333 | Rare:17 | ||||
chr1:2229320-2229399 | Rare:29; Clinvar:2; Clinvar (benign):2 | ||||
chr1:2551665-2551708 | Common:1; Rare:7 | ||||
chr1:2551784-2552050 | Common:3; Rare:64 | ||||
chr1:2552053-2552182 | Common:3; Rare:26 | ||||
chr1:2585334-2585640 | Common:3; Rare:69 |