Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150321406-150321602 | Rare:62; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363891-150364225 | Common:4; Rare:113 | ||||
chr1:150364537-150364724 | Common:1; Rare:59 | ||||
chr1:150487239-150487462 | Common:3; Rare:58; Clinvar (benign):3 | ||||
chr1:150507967-150508129 | Common:3; Rare:33 | ||||
chr1:150549202-150549434 | Rare:61 | ||||
chr1:150551986-150552291 | Common:1; Rare:62 | ||||
chr1:150557880-150558014 | Rare:48; Clinvar:3 | ||||
chr1:150558190-150558539 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
chr1:150578473-150578748 | Common:1; Rare:84 | ||||
chr1:150578819-150579110 | Common:3; Rare:119 | ||||
chr1:150579111-150579331 | Rare:91 | ||||
chr1:150579345-150579507 | Common:1; Rare:63 | ||||
chr1:150579517-150579837 | Common:10; Rare:112 | ||||
chr1:150629061-150629314 | Rare:76 |