Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149927758-149927917 | Common:1; Rare:63; Clinvar (benign):5 | ||||
chr1:150010697-150010834 | Common:1; Rare:34 | ||||
chr1:150067123-150067350 | Common:4; Rare:39 | ||||
chr1:150067610-150067905 | Common:1; Rare:83 | ||||
chr1:150149581-150149705 | Common:1; Rare:34 | ||||
chr1:150150111-150150265 | Common:2; Rare:50 | ||||
chr1:150236134-150236466 | Rare:65 | ||||
chr1:150257683-150257903 | Rare:53 | ||||
chr1:150293805-150293927 | Common:1; Rare:43 | ||||
chr1:150321406-150321608 | Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363874-150364201 | Common:6; Rare:112 | ||||
chr1:150364572-150364714 | Common:1; Rare:50 | ||||
chr1:150579162-150579350 | Rare:83 | ||||
chr1:150579595-150579846 | Common:9; Rare:78 | ||||
chr1:150629107-150629374 | Common:1; Rare:76 |