Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150067589-150067840 | Common:1; Rare:67 | ||||
chr1:150149768-150149917 | Rare:63 | ||||
chr1:150234605-150234908 | Rare:58 | ||||
chr1:150236081-150236406 | Rare:74 | ||||
chr1:150236440-150236760 | Common:3; Rare:53 | ||||
chr1:150268282-150268682 | Rare:116 | ||||
chr1:150268976-150269205 | Rare:53 | ||||
chr1:150293749-150293927 | Common:1; Rare:60 | ||||
chr1:150321384-150321629 | Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363915-150364375 | Common:4; Rare:143 | ||||
chr1:150364541-150364896 | Common:2; Rare:102 | ||||
chr1:150487173-150487468 | Common:6; Rare:73; Clinvar (benign):3 | ||||
chr1:150507779-150508251 | Common:8; Rare:171 | ||||
chr1:150548860-150549100 | Common:1; Rare:60 | ||||
chr1:150549173-150549446 | Rare:69 |