Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25338190-25338447 | Common:1; Rare:91 | ||||
chr1:25819889-25820029 | Common:3; Rare:44 | ||||
chr1:25906392-25906601 | Rare:80 | ||||
chr1:26111079-26111217 | Rare:44 | ||||
chr1:26234005-26234236 | Common:1; Rare:79 | ||||
chr1:26279961-26280162 | Rare:115 | ||||
chr1:26432091-26432422 | Common:5; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472247-26472521 | Common:4; Rare:86 | ||||
chr1:26900448-26900492 | Rare:17 | ||||
chr1:26921554-26921855 | Common:3; Rare:94 | ||||
chr1:27322034-27322332 | Common:1; Rare:107 | ||||
chr1:27772878-27773317 | Common:1; Rare:139 | ||||
chr1:28235956-28236227 | Common:3; Rare:86 | ||||
chr1:28328894-28329073 | Common:1; Rare:57 | ||||
chr1:28505869-28506050 | Common:1; Rare:76 |