Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:100132560-100132770 | Common:1; Rare:71 | ||||
chr1:100132786-100133249 | Common:19; Rare:946 | ||||
chr1:100133174-100133574 | Common:3; Rare:154 | ||||
chr1:100249710-100250151 | Common:20; Rare:579; Clinvar:10; Clinvar (benign):10; Clinvar (pathogenic):4 | ||||
chr1:100265515-100265937 | Common:6; Rare:145 | ||||
chr1:100266028-100266950 | Common:27; Rare:951 | ||||
chr1:100350890-100351520 | Common:5; Rare:253 | ||||
chr1:100351480-100351900 | Common:20; Rare:595 | ||||
chr1:100352062-100352754 | Common:7; Rare:540 | ||||
chr1:100352905-100353550 | Common:5; Rare:229; Clinvar (benign):3 | ||||
chr1:100894540-100894970 | Common:9; Rare:357 | ||||
chr1:100894913-100895169 | Common:1; Rare:70 | ||||
chr1:100895073-100895458 | Common:6; Rare:159 | ||||
chr1:100895807-100896233 | Common:1; Rare:459 | ||||
chr1:100896278-100897047 | Common:4; Rare:234 |