Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:778585-778819 | Common:5; Rare:100 | ||||
chr1:827468-827688 | Common:2; Rare:89 | ||||
chr1:9263332-9263633 | Common:3; Rare:111; Clinvar (pathogenic):1 | ||||
chr1:9687535-9687633 | Common:1; Rare:23 | ||||
chr1:10641733-10641979 | Common:2; Rare:49 | ||||
chr1:10699519-10699671 | Common:1; Rare:22 | ||||
chr1:12619094-12619110 | Rare:5 | ||||
chr1:14419969-14420024 | Rare:21 | ||||
chr1:15834860-15835158 | Common:2; Rare:129 | ||||
chr1:15835840-15836120 | Common:6; Rare:127 | ||||
chr1:16499217-16499368 | Rare:70 | ||||
chr1:16644644-16644809 | Common:1; Rare:3 | ||||
chr1:25875503-25875771 | Rare:69 | ||||
chr1:32192067-32192335 | Common:1; Rare:59 | ||||
chr1:32240275-32240541 | Common:2; Rare:57 |