Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42846401-42846635 | Common:1; Rare:64 | ||||
chr1:43367946-43368213 | Rare:69 | ||||
chr1:43389781-43389945 | Common:3; Rare:62 | ||||
chr1:45340384-45340682 | Common:1; Rare:67; Clinvar:1 | ||||
chr1:45500025-45500335 | Common:2; Rare:71; Clinvar:4; Clinvar (pathogenic):2 | ||||
chr1:45521901-45522069 | Rare:60 | ||||
chr1:45583958-45584051 | Rare:33 | ||||
chr1:45687059-45687350 | Common:1; Rare:75 | ||||
chr1:45688049-45688245 | Common:1; Rare:55 | ||||
chr1:46198406-46198497 | Common:1; Rare:34; Clinvar:1 | ||||
chr1:46303369-46303726 | Common:2; Rare:88 | ||||
chr1:46340985-46341170 | Common:1; Rare:44 | ||||
chr1:51236153-51236322 | Common:3; Rare:65 | ||||
chr1:52056104-52056335 | Common:1; Rare:69 | ||||
chr1:53220571-53220690 | Common:1; Rare:58 |