Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23691739-23691826 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
chr1:23778248-23778492 | Common:9; Rare:127 | ||||
chr1:23800732-23800959 | Common:1; Rare:80 | ||||
chr1:23825405-23825537 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959603-23959854 | Common:2; Rare:67 | ||||
chr1:23980203-23980517 | Rare:86 | ||||
chr1:24413691-24413897 | Common:1; Rare:46 | ||||
chr1:24415633-24415827 | Common:1; Rare:55 | ||||
chr1:24642981-24643335 | Common:2; Rare:109 | ||||
chr1:25232442-25232668 | Rare:93 | ||||
chr1:25247419-25247639 | Common:2; Rare:84 | ||||
chr1:25338207-25338447 | Common:1; Rare:83 | ||||
chr1:25819895-25820021 | Common:2; Rare:40 | ||||
chr1:25859370-25859556 | Common:2; Rare:76 | ||||
chr1:25892556-25892716 | Common:3; Rare:31 |