Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150321398-150321599 | Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363951-150364232 | Common:3; Rare:99 | ||||
chr1:150364550-150364717 | Common:1; Rare:58 | ||||
chr1:150487231-150487446 | Common:4; Rare:50; Clinvar (benign):3 | ||||
chr1:150578532-150578699 | Common:1; Rare:46 | ||||
chr1:150579131-150579311 | Rare:76 | ||||
chr1:150579595-150579846 | Common:9; Rare:78 | ||||
chr1:150629107-150629314 | Rare:58 | ||||
chr1:150629466-150629858 | Common:1; Rare:91 | ||||
chr1:150697181-150697494 | Common:2; Rare:65 | ||||
chr1:150876573-150876917 | Common:5; Rare:126 | ||||
chr1:150926183-150926327 | Rare:41 | ||||
chr1:150926342-150926452 | Rare:34 | ||||
chr1:151006801-151006935 | Rare:29 | ||||
chr1:151008314-151008533 | Common:1; Rare:73 |