Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1099082-1099223 | Common:6; Rare:17 | ||||
chr1:1233489-1233584 | Rare:36 | ||||
chr1:1360655-1360692 | Rare:5 | ||||
chr1:1400105-1400244 | Rare:54 | ||||
chr1:1401337-1401521 | Rare:44 | ||||
chr1:1570437-1570617 | Common:2; Rare:40 | ||||
chr1:1598037-1598104 | Common:1; Rare:20 | ||||
chr1:1808952-1809181 | Common:1; Rare:44 | ||||
chr1:1844224-1844320 | Rare:15 | ||||
chr1:1872099-1872386 | Common:1; Rare:55 | ||||
chr1:2428510-2428821 | Common:2; Rare:81 | ||||
chr1:2546265-2546400 | Common:1; Rare:37 | ||||
chr1:4668794-4668823 | Rare:6 | ||||
chr1:6198578-6198615 | Rare:7 | ||||
chr1:6470845-6471079 | Common:4; Rare:89; Clinvar:5; Clinvar (benign):4 |