Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:28648333-28648622 | Common:4; Rare:102 | ||||
chr1:32240297-32240541 | Common:2; Rare:52 | ||||
chr1:36296490-36296658 | Rare:25 | ||||
chr1:40064225-40064558 | Rare:83 | ||||
chr1:43348710-43348955 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
chr1:44721904-44722164 | Common:4; Rare:71 | ||||
chr1:45205844-45205946 | Common:1; Rare:30 | ||||
chr1:51783761-51784024 | Rare:48 | ||||
chr1:51790531-51790872 | Common:2; Rare:96 | ||||
chr1:51794822-51794928 | Common:1; Rare:18 | ||||
chr1:56577970-56577973 | |||||
chr1:58576122-58576133 | Rare:2; Clinvar:1 | ||||
chr1:58783547-58783681 | Rare:28 | ||||
chr1:58903726-58903997 | Rare:86 | ||||
chr1:63322173-63322410 | Common:3; Rare:70 |