Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150321413-150321613 | Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150364423-150364747 | Common:1; Rare:91 | ||||
chr1:150508030-150508276 | Common:2; Rare:60 | ||||
chr1:150578540-150579179 | Common:6; Rare:218 | ||||
chr1:150579183-150579659 | Common:2; Rare:192 | ||||
chr1:150629075-150629412 | Common:1; Rare:106 | ||||
chr1:150629534-150629827 | Rare:58 | ||||
chr1:150765762-150766046 | Common:1; Rare:33 | ||||
chr1:150808234-150808373 | Rare:35; Clinvar:2 | ||||
chr1:150876638-150876980 | Rare:101 | ||||
chr1:150926303-150926524 | Rare:58 | ||||
chr1:150967664-150967868 | Common:1; Rare:50 | ||||
chr1:150974653-150974886 | Common:2; Rare:68 | ||||
chr1:150982186-150982345 | Common:2; Rare:27 | ||||
chr1:151008197-151008566 | Common:2; Rare:95 |