Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20661340-20661709 | Common:3; Rare:133; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786616-20786856 | Rare:91 | ||||
chr1:20787244-20787440 | Rare:94 | ||||
chr1:21345467-21345640 | Common:2; Rare:68 | ||||
chr1:21440061-21440189 | Common:1; Rare:29 | ||||
chr1:21783086-21783295 | Common:2; Rare:76 | ||||
chr1:22451806-22451868 | Rare:29 | ||||
chr1:23344233-23344544 | Common:2; Rare:102 | ||||
chr1:23368200-23368513 | Common:1; Rare:92 | ||||
chr1:23424698-23424918 | Rare:57 | ||||
chr1:23559411-23559643 | Common:1; Rare:101 | ||||
chr1:23691739-23691826 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
chr1:23778247-23778569 | Common:10; Rare:145 | ||||
chr1:23791025-23791231 | Rare:68 | ||||
chr1:23825405-23825534 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |