Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:65147440-65147695 | Common:1; Rare:77 | ||||
chr1:65147813-65148212 | Common:4; Rare:93 | ||||
chr1:65148712-65148995 | Common:3; Rare:79 | ||||
chr1:65254342-65254599 | Common:1; Rare:86 | ||||
chr1:65254677-65254708 | Rare:8 | ||||
chr1:65420108-65420800 | Common:7; Rare:185; Clinvar:2; Clinvar (benign):1 | ||||
chr1:65420941-65421205 | Rare:51 | ||||
chr1:66924730-66925062 | Common:3; Rare:147 | ||||
chr1:66925173-66925533 | Common:2; Rare:115 | ||||
chr1:66930063-66930458 | Rare:140 | ||||
chr1:66930512-66930579 | Common:1; Rare:17 | ||||
chr1:67053625-67053911 | Common:4; Rare:129; Clinvar (pathogenic):1 | ||||
chr1:67053922-67054036 | Rare:55 | ||||
chr1:67054083-67054263 | Common:2; Rare:39 | ||||
chr1:67054297-67054425 | Common:3; Rare:23 |