Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40508674-40508816 | Common:4; Rare:39 | ||||
chr1:40531509-40531586 | Rare:22 | ||||
chr1:41242106-41242353 | Rare:70 | ||||
chr1:42335143-42335346 | Common:4; Rare:108 | ||||
chr1:42456469-42456586 | Rare:57 | ||||
chr1:42682158-42682442 | Common:2; Rare:71 | ||||
chr1:42766562-42766725 | Rare:40; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:42766996-42767303 | Common:4; Rare:102; Clinvar (benign):1 | ||||
chr1:42816932-42817141 | Common:1; Rare:59 | ||||
chr1:42817203-42817624 | Rare:128 | ||||
chr1:42846412-42846636 | Common:1; Rare:60 | ||||
chr1:42958814-42959063 | Common:3; Rare:70; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43358690-43359006 | Common:7; Rare:99 | ||||
chr1:43367946-43368221 | Rare:71 | ||||
chr1:43389757-43389945 | Common:3; Rare:83 |