Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24930250-24930500 | Rare:71 | ||||
chr1:25232007-25232146 | Common:2; Rare:71 | ||||
chr1:25232230-25232727 | Common:1; Rare:708 | ||||
chr1:25245438-25247317 | Common:25; Rare:1515 | ||||
chr1:25247331-25247905 | Common:24; Rare:908 | ||||
chr1:25267440-25268100 | Common:35; Rare:454 | ||||
chr1:25272435-25272850 | Common:1; Rare:217 | ||||
chr1:25336478-25337230 | Common:5; Rare:235 | ||||
chr1:25337672-25338804 | Common:15; Rare:872 | ||||
chr1:25338760-25339155 | Common:6; Rare:111 | ||||
chr1:25419521-25420872 | Common:14; Rare:486; Clinvar (benign):2 | ||||
chr1:25429930-25430650 | Common:29; Rare:637 | ||||
chr1:25430551-25431013 | Common:15; Rare:468 | ||||
chr1:25431230-25431670 | Common:2; Rare:167 | ||||
chr1:25543281-25543699 | Common:3; Rare:323; Clinvar:15 |