Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23558924-23559246 | Common:5; Rare:149 | ||||
chr1:23559248-23559657 | Common:1; Rare:182 | ||||
chr1:23778250-23778550 | Common:10; Rare:140 | ||||
chr1:23785555-23785765 | Common:1; Rare:49 | ||||
chr1:23791066-23791247 | Rare:55 | ||||
chr1:23796760-23796801 | Rare:11; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:23799459-23799787 | Common:1; Rare:63 | ||||
chr1:23800723-23800957 | Common:1; Rare:82 | ||||
chr1:23825362-23825537 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr1:23868240-23868445 | Common:6; Rare:67; Clinvar:2; Clinvar (benign):5 | ||||
chr1:23959641-23960005 | Common:2; Rare:89 | ||||
chr1:23960044-23960105 | Rare:25 | ||||
chr1:23960165-23960468 | Common:3; Rare:71 | ||||
chr1:23960930-23961389 | Common:5; Rare:73 | ||||
chr1:23980160-23980486 | Rare:86 |