Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19596922-19597109 | Common:2; Rare:95 | ||||
chr1:20485818-20486325 | Common:1; Rare:96 | ||||
chr1:20661162-20661290 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
chr1:20661343-20661699 | Common:3; Rare:126; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20732192-20732415 | Rare:48 | ||||
chr1:20787196-20787473 | Rare:130 | ||||
chr1:21176798-21177062 | Rare:74 | ||||
chr1:21279298-21279482 | Rare:65 | ||||
chr1:21290179-21290459 | Common:1; Rare:60 | ||||
chr1:21345443-21345674 | Common:3; Rare:82 | ||||
chr1:21440039-21440242 | Common:1; Rare:44 | ||||
chr1:21783082-21783277 | Common:2; Rare:71 | ||||
chr1:21833360-21833526 | Rare:42; Clinvar (benign):1 | ||||
chr1:22052533-22052751 | Common:2; Rare:73 | ||||
chr1:23019329-23019569 | Rare:86 |