Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45550709-45551104 | Common:3; Rare:98 | ||||
chr1:45566643-45566902 | Common:3; Rare:64 | ||||
chr1:45583931-45584066 | Rare:51 | ||||
chr1:45686452-45686655 | Rare:71 | ||||
chr1:45687036-45687357 | Common:2; Rare:84 | ||||
chr1:45688049-45688216 | Common:1; Rare:41 | ||||
chr1:45750615-45750821 | Rare:77 | ||||
chr1:45803455-45803653 | Common:2; Rare:76 | ||||
chr1:46133024-46133069 | Rare:15 | ||||
chr1:46198346-46198604 | Common:6; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
chr1:46303124-46303775 | Common:3; Rare:194 | ||||
chr1:46340606-46340821 | Common:3; Rare:56 | ||||
chr1:46341066-46341321 | Common:2; Rare:60 | ||||
chr1:46604186-46604443 | Common:1; Rare:69 | ||||
chr1:46616781-46617028 | Common:2; Rare:54 |