Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19251510-19251838 | Common:6; Rare:107 | ||||
chr1:19312038-19312329 | Common:8; Rare:145 | ||||
chr1:19799878-19799987 | Common:1; Rare:43 | ||||
chr1:20508097-20508200 | Common:2; Rare:37 | ||||
chr1:20661346-20661687 | Common:3; Rare:123; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786644-20786861 | Rare:87 | ||||
chr1:20787259-20787447 | Rare:88 | ||||
chr1:21176878-21177170 | Common:1; Rare:78 | ||||
chr1:21345476-21345723 | Common:2; Rare:89 | ||||
chr1:21783086-21783279 | Common:2; Rare:69 | ||||
chr1:22451645-22451865 | Common:1; Rare:69 | ||||
chr1:23559451-23559648 | Common:1; Rare:83 | ||||
chr1:23791717-23791979 | Rare:38 | ||||
chr1:23800730-23800959 | Common:1; Rare:80 | ||||
chr1:23959641-23959861 | Common:2; Rare:60 |