Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39026244-39026397 | Common:1; Rare:41 | ||||
chr1:40257910-40258264 | Common:4; Rare:95; Clinvar:7 | ||||
chr1:40692051-40692104 | Rare:22 | ||||
chr1:42682154-42682424 | Common:2; Rare:70 | ||||
chr1:42767016-42767297 | Common:4; Rare:85 | ||||
chr1:42846401-42846650 | Common:1; Rare:69 | ||||
chr1:42958785-42959049 | Common:3; Rare:70; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43368013-43368212 | Rare:55 | ||||
chr1:43389754-43389910 | Common:3; Rare:65 | ||||
chr1:43707337-43707566 | Common:2; Rare:66 | ||||
chr1:43978911-43979253 | Common:2; Rare:93 | ||||
chr1:43979850-43979971 | Rare:30 | ||||
chr1:44775776-44776138 | Common:2; Rare:132 | ||||
chr1:44986550-44986825 | Common:2; Rare:52; Clinvar (benign):1 | ||||
chr1:45500088-45500351 | Common:1; Rare:66; Clinvar:4; Clinvar (pathogenic):3 |