Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23019327-23019517 | Rare:61 | ||||
chr1:23344211-23344417 | Common:2; Rare:81 | ||||
chr1:23368200-23368530 | Common:1; Rare:97 | ||||
chr1:23559348-23559643 | Common:1; Rare:128 | ||||
chr1:23778250-23778596 | Common:10; Rare:146 | ||||
chr1:23778652-23778688 | Rare:6 | ||||
chr1:23793750-23793896 | Rare:44 | ||||
chr1:23800741-23800929 | Common:1; Rare:60 | ||||
chr1:23868280-23868479 | Common:4; Rare:55; Clinvar:1; Clinvar (benign):3 | ||||
chr1:23959641-23959999 | Common:2; Rare:86 | ||||
chr1:23980191-23980497 | Rare:79 | ||||
chr1:24319606-24319792 | Rare:33 | ||||
chr1:24322373-24322570 | Common:1; Rare:41 | ||||
chr1:24322869-24322914 | Rare:8 | ||||
chr1:24342650-24343025 | Common:3; Rare:126; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |