Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:31644843-31644982 | Common:3; Rare:50 | ||||
chr1:32205542-32205675 | Common:1; Rare:51 | ||||
chr1:32291986-32292158 | Rare:65 | ||||
chr1:32394419-32394656 | Common:1; Rare:63 | ||||
chr1:32650926-32651300 | Common:2; Rare:143 | ||||
chr1:32753844-32754172 | Common:3; Rare:116 | ||||
chr1:32817270-32817686 | Rare:111; Clinvar:5; Clinvar (benign):1 | ||||
chr1:32895303-32895593 | Rare:99 | ||||
chr1:32895612-32895914 | Common:2; Rare:93 | ||||
chr1:33182034-33182222 | Rare:45 | ||||
chr1:34759634-34759803 | Common:1; Rare:31 | ||||
chr1:34781535-34781744 | Common:1; Rare:35; Clinvar:3; Clinvar (benign):1 | ||||
chr1:35192441-35192723 | Common:2; Rare:88 | ||||
chr1:35557636-35557845 | Common:2; Rare:81 | ||||
chr1:35930848-35931143 | Common:2; Rare:112 |