Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20786626-20786842 | Rare:84 | ||||
chr1:20787196-20787450 | Rare:119 | ||||
chr1:21176878-21177065 | Rare:41 | ||||
chr1:21345484-21345655 | Rare:65 | ||||
chr1:23368854-23368982 | Common:1; Rare:44 | ||||
chr1:23559487-23559648 | Common:1; Rare:65 | ||||
chr1:23791066-23791231 | Rare:51 | ||||
chr1:23800723-23800948 | Common:1; Rare:78 | ||||
chr1:23825421-23825509 | Common:2; Rare:34; Clinvar:1; Clinvar (benign):2 | ||||
chr1:23959641-23959854 | Common:2; Rare:57 | ||||
chr1:24413714-24413868 | Common:1; Rare:35 | ||||
chr1:24415518-24415829 | Common:3; Rare:78 | ||||
chr1:24642890-24643350 | Common:2; Rare:151 | ||||
chr1:25232444-25232657 | Rare:86 | ||||
chr1:25247421-25247613 | Common:2; Rare:69 |