Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:633775-634021 | Common:5; Rare:91 | ||||
chr1:778620-778819 | Common:3; Rare:80 | ||||
chr1:827472-827809 | Common:3; Rare:111 | ||||
chr1:1636741-1636968 | Common:1; Rare:112 | ||||
chr1:2229563-2229667 | Rare:37; Clinvar:1; Clinvar (benign):4 | ||||
chr1:7809776-7810018 | Common:5; Rare:68; Clinvar (pathogenic):2 | ||||
chr1:8121337-8121649 | Common:3; Rare:58 | ||||
chr1:8378304-8378603 | Common:1; Rare:55 | ||||
chr1:9182107-9182199 | Rare:24 | ||||
chr1:9687513-9687640 | Common:1; Rare:35 | ||||
chr1:12619042-12619236 | Rare:39 | ||||
chr1:12619926-12620017 | Rare:17 | ||||
chr1:15834831-15835133 | Common:2; Rare:136 | ||||
chr1:15835793-15836134 | Common:6; Rare:165 | ||||
chr1:16499217-16499390 | Rare:83 |