Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21833267-21833616 | Common:3; Rare:100; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:21838823-21839482 | Common:2; Rare:201; Clinvar:7; Clinvar (benign):5 | ||||
chr1:21847744-21848097 | Common:3; Rare:122; Clinvar:5; Clinvar (benign):1 | ||||
chr1:21854609-21854986 | Common:2; Rare:143; Clinvar:6; Clinvar (benign):2 | ||||
chr1:21874614-21875044 | Common:2; Rare:134; Clinvar:1; Clinvar (benign):2 | ||||
chr1:21875627-21876050 | Common:4; Rare:142; Clinvar:6; Clinvar (benign):3 | ||||
chr1:23369812-23369931 | Rare:23 | ||||
chr1:23559325-23559643 | Common:1; Rare:140 | ||||
chr1:23559645-23559670 | Common:1; Rare:11 | ||||
chr1:23743204-23743544 | Rare:120 | ||||
chr1:23791101-23791247 | Rare:42 | ||||
chr1:23825388-23825528 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959608-23959916 | Common:2; Rare:81 | ||||
chr1:23980189-23980466 | Rare:73 | ||||
chr1:24415633-24415812 | Common:1; Rare:53 |