Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15776136-15776505 | Rare:77 | ||||
chr1:15834859-15835133 | Common:2; Rare:121 | ||||
chr1:15835805-15836081 | Common:6; Rare:129 | ||||
chr1:15899570-15899809 | Common:1; Rare:46 | ||||
chr1:16131720-16132070 | Common:1; Rare:96; Clinvar (benign):3 | ||||
chr1:16155015-16155256 | Common:1; Rare:52 | ||||
chr1:16241056-16241117 | Common:1; Rare:3 | ||||
chr1:16313416-16313692 | Common:1; Rare:45 | ||||
chr1:16351552-16351603 | Rare:14 | ||||
chr1:16618294-16618439 | Common:2; Rare:3 | ||||
chr1:16618486-16618750 | Common:5; Rare:4 | ||||
chr1:16644650-16644791 | Common:1; Rare:2 | ||||
chr1:17189645-17189802 | Common:1; Rare:23 | ||||
chr1:17192428-17192658 | Common:1; Rare:48 | ||||
chr1:18209543-18209650 | Common:2; Rare:19 |