Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40508685-40508773 | Common:3; Rare:24 | ||||
chr1:40531497-40531653 | Rare:38 | ||||
chr1:40691520-40691843 | Common:2; Rare:153 | ||||
chr1:42335104-42335323 | Common:2; Rare:107 | ||||
chr1:42456013-42456577 | Common:1; Rare:162 | ||||
chr1:42456843-42456963 | Common:1; Rare:47; Clinvar (pathogenic):1 | ||||
chr1:42658312-42658482 | Rare:52 | ||||
chr1:42682606-42682731 | Common:1; Rare:52 | ||||
chr1:42683257-42683465 | Common:3; Rare:85 | ||||
chr1:42767028-42767303 | Common:3; Rare:79 | ||||
chr1:42816981-42817136 | Common:1; Rare:43 | ||||
chr1:42817198-42817454 | Rare:92 | ||||
chr1:42846412-42846634 | Common:1; Rare:58 | ||||
chr1:42958858-42958981 | Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
chr1:43358662-43358986 | Common:7; Rare:102 |