Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24642981-24643339 | Common:2; Rare:110 | ||||
chr1:24745359-24745447 | Common:1; Rare:35 | ||||
chr1:25232460-25232657 | Rare:76 | ||||
chr1:25247061-25247167 | Rare:33 | ||||
chr1:25247419-25247741 | Common:4; Rare:113 | ||||
chr1:25338085-25338363 | Common:1; Rare:82 | ||||
chr1:25819887-25820032 | Common:3; Rare:44 | ||||
chr1:26279934-26280201 | Rare:144 | ||||
chr1:26317798-26318090 | Common:3; Rare:57 | ||||
chr1:26318381-26318658 | Common:1; Rare:51 | ||||
chr1:26432162-26432426 | Common:4; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26695933-26696048 | Rare:38 | ||||
chr1:26890248-26890391 | Common:1; Rare:62 | ||||
chr1:26900432-26900513 | Rare:31 | ||||
chr1:26921529-26921827 | Common:3; Rare:94 |