Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:28648308-28648600 | Common:4; Rare:84 | ||||
chr1:28983823-28983911 | Common:1; Rare:17 | ||||
chr1:29039065-29039412 | Common:1; Rare:82 | ||||
chr1:32226207-32226504 | Rare:75 | ||||
chr1:33331346-33331719 | Rare:62 | ||||
chr1:39158562-39158916 | Common:1; Rare:72 | ||||
chr1:39968376-39968745 | Common:2; Rare:80 | ||||
chr1:40071164-40071730 | Common:3; Rare:116 | ||||
chr1:40861161-40861182 | Rare:11 | ||||
chr1:43603438-43603727 | Rare:79 | ||||
chr1:43619843-43620131 | Rare:80 | ||||
chr1:44776194-44776492 | Common:1; Rare:64 | ||||
chr1:45514511-45514987 | Rare:134 | ||||
chr1:46195831-46196010 | Rare:53; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr1:46718493-46718518 | Common:1; Rare:3 |