Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:100037911-100038220 | Common:1; Rare:115 | ||||
chr1:100132601-100132778 | Common:1; Rare:44 | ||||
chr1:100132818-100133210 | Common:3; Rare:149 | ||||
chr1:100133399-100133444 | Rare:6 | ||||
chr1:100249732-100250055 | Common:4; Rare:109; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:100266055-100266326 | Common:3; Rare:95 | ||||
chr1:100266711-100266731 | Rare:3 | ||||
chr1:100266764-100266798 | Rare:8 | ||||
chr1:100351296-100351468 | Rare:41 | ||||
chr1:100351583-100351733 | Common:2; Rare:51 | ||||
chr1:100352151-100352563 | Common:1; Rare:95 | ||||
chr1:100719603-100719779 | Common:1; Rare:43 | ||||
chr1:100894639-100894954 | Common:2; Rare:75 | ||||
chr1:100895118-100895454 | Common:2; Rare:63 | ||||
chr1:100895881-100896271 | Rare:105 |