Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42456219-42456572 | Common:1; Rare:104 | ||||
chr1:42658317-42658436 | Rare:34 | ||||
chr1:42682122-42682442 | Common:2; Rare:86 | ||||
chr1:42683255-42683465 | Common:3; Rare:86 | ||||
chr1:42767010-42767293 | Common:4; Rare:88; Clinvar (benign):1 | ||||
chr1:42817009-42817136 | Common:1; Rare:32 | ||||
chr1:42817203-42817351 | Rare:62 | ||||
chr1:42846401-42846635 | Common:1; Rare:64 | ||||
chr1:42958845-42959042 | Common:2; Rare:52; Clinvar:4; Clinvar (benign):3 | ||||
chr1:43172233-43172341 | Common:1; Rare:58 | ||||
chr1:43285536-43285818 | Common:5; Rare:50 | ||||
chr1:43367942-43368185 | Rare:60 | ||||
chr1:43389733-43389945 | Common:3; Rare:95 | ||||
chr1:43946607-43946983 | Rare:100 | ||||
chr1:43974804-43974967 | Common:2; Rare:47 |