Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45499993-45500341 | Common:2; Rare:81; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521827-45522074 | Common:1; Rare:98 | ||||
chr1:45550747-45551098 | Common:3; Rare:82 | ||||
chr1:45583930-45584095 | Rare:64 | ||||
chr1:45687017-45687357 | Common:2; Rare:89 | ||||
chr1:45688049-45688242 | Common:1; Rare:53 | ||||
chr1:45750615-45750821 | Rare:77 | ||||
chr1:46198384-46198510 | Common:1; Rare:50; Clinvar:1 | ||||
chr1:46303131-46303240 | Common:1; Rare:25 | ||||
chr1:46303245-46303782 | Common:2; Rare:167 | ||||
chr1:46340651-46340821 | Common:3; Rare:46 | ||||
chr1:46604219-46604448 | Common:1; Rare:57 | ||||
chr1:46718332-46718577 | Common:2; Rare:52 | ||||
chr1:47229354-47229688 | Common:1; Rare:60 | ||||
chr1:47231256-47231400 | Rare:22 |