Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42766959-42767303 | Common:4; Rare:116; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:42817004-42817136 | Common:1; Rare:32 | ||||
chr1:42817198-42817385 | Rare:77 | ||||
chr1:42846406-42846642 | Common:1; Rare:64 | ||||
chr1:42958647-42959100 | Common:4; Rare:115; Clinvar:6; Clinvar (benign):8 | ||||
chr1:43285542-43285650 | Common:1; Rare:19 | ||||
chr1:43358666-43359000 | Common:7; Rare:102 | ||||
chr1:43367923-43368152 | Rare:56 | ||||
chr1:43386614-43386924 | Rare:79 | ||||
chr1:43389733-43389971 | Common:4; Rare:105; Clinvar:1 | ||||
chr1:43605429-43605598 | Common:1; Rare:65 | ||||
chr1:43946553-43946983 | Rare:115 | ||||
chr1:43969865-43970023 | Rare:40 | ||||
chr1:43974808-43974997 | Common:3; Rare:54 | ||||
chr1:44031348-44031665 | Common:2; Rare:64 |