Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:147541297-147541561 | Common:1; Rare:43 | ||||
chr1:147600084-147600245 | Rare:70 | ||||
chr1:148951942-148952159 | Common:3; Rare:57 | ||||
chr1:148952252-148952603 | Common:5; Rare:102 | ||||
chr1:148952607-148952642 | Rare:2 | ||||
chr1:149390434-149390634 | Rare:25 | ||||
chr1:149812300-149812560 | Common:2; Rare:107 | ||||
chr1:149842748-149842984 | Rare:3 | ||||
chr1:149850826-149851078 | Rare:1 | ||||
chr1:149886170-149886364 | Rare:50 | ||||
chr1:149886632-149887256 | Common:3; Rare:229 | ||||
chr1:149887885-149888215 | Rare:101 | ||||
chr1:149927748-149927910 | Common:1; Rare:64; Clinvar (benign):5 | ||||
chr1:150010464-150010484 | Rare:3 | ||||
chr1:150010511-150010948 | Common:4; Rare:110 |