Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236523833-236524060 | Common:3; Rare:59 | ||||
chr1:236686630-236686799 | Common:1; Rare:55; Clinvar:7; Clinvar (benign):6 | ||||
chr1:241519656-241519977 | Common:2; Rare:105; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):4 | ||||
chr1:243255183-243255351 | Common:1; Rare:33 | ||||
chr1:243255776-243256104 | Rare:89; Clinvar:4 | ||||
chr1:244835160-244835337 | Rare:70 | ||||
chr1:244835562-244835752 | Common:2; Rare:85; Clinvar (benign):5 | ||||
chr1:244863975-244864382 | Common:1; Rare:124; Clinvar:3; Clinvar (benign):5 | ||||
chr1:244864391-244864693 | Rare:118 | ||||
chr1:246566188-246566584 | Common:1; Rare:129 | ||||
chr1:248858940-248859154 | Rare:85 | ||||
chr10:134753-134823 | Rare:18 | ||||
chr10:988279-988470 | Common:1; Rare:70 | ||||
chr10:1048880-1049092 | Common:2; Rare:109 | ||||
chr10:1056702-1056872 | Common:3; Rare:63 |