Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25247383-25247871 | Common:4; Rare:165 | ||||
chr1:25338110-25338411 | Common:1; Rare:97 | ||||
chr1:25338546-25338658 | Common:1; Rare:20 | ||||
chr1:25338817-25338927 | Common:1; Rare:21 | ||||
chr1:25430095-25430370 | Common:5; Rare:91 | ||||
chr1:25430626-25431083 | Common:4; Rare:141 | ||||
chr1:25543459-25543686 | Common:1; Rare:86; Clinvar:5 | ||||
chr1:25800012-25800245 | Rare:87; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:25800406-25800465 | Rare:11; Clinvar:1; Clinvar (benign):1 | ||||
chr1:25819763-25820061 | Common:6; Rare:99 | ||||
chr1:25820062-25820248 | Common:1; Rare:48 | ||||
chr1:25820751-25820916 | Common:2; Rare:47 | ||||
chr1:25859298-25859633 | Common:3; Rare:137 | ||||
chr1:25892279-25892465 | Common:1; Rare:26 | ||||
chr1:25892572-25892753 | Common:2; Rare:32 |