Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:2194698-2194834 | Rare:47 | ||||
chr1:2391529-2391873 | Common:2; Rare:128 | ||||
chr1:2526573-2526704 | Common:3; Rare:51 | ||||
chr1:3068869-3069234 | Common:1; Rare:84 | ||||
chr1:3624747-3625036 | Common:1; Rare:99 | ||||
chr1:3900219-3900406 | Common:11; Rare:87 | ||||
chr1:5992394-5992766 | Common:4; Rare:121; Clinvar:6 | ||||
chr1:6208680-6208872 | Common:1; Rare:52 | ||||
chr1:6579803-6580024 | Common:3; Rare:68 | ||||
chr1:6701769-6701972 | Rare:60 | ||||
chr1:7954141-7954293 | Rare:42 | ||||
chr1:7961442-7961780 | Common:4; Rare:118; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8026177-8026493 | Common:3; Rare:145 | ||||
chr1:8878587-8878823 | Rare:121 | ||||
chr1:9942783-9942970 | Common:1; Rare:37 |