Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150364410-150364897 | Common:6; Rare:536 | ||||
chr1:150487140-150487548 | Common:36; Rare:496; Clinvar:1; Clinvar (benign):21 | ||||
chr1:150507800-150508200 | Common:9; Rare:161 | ||||
chr1:150509118-150509518 | Common:6; Rare:96 | ||||
chr1:150548629-150549029 | Common:4; Rare:86 | ||||
chr1:150549033-150549620 | Rare:571 | ||||
chr1:150549537-150549937 | Common:4; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
chr1:150551168-150553079 | Common:20; Rare:1022; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150578368-150579149 | Common:22; Rare:728 | ||||
chr1:150579162-150579500 | Common:1; Rare:190 | ||||
chr1:150579507-150580169 | Common:75; Rare:791 | ||||
chr1:150629044-150629420 | Common:3; Rare:533 | ||||
chr1:150629420-150629960 | Common:11; Rare:586 | ||||
chr1:150629981-150630389 | Common:3; Rare:110 | ||||
chr1:150697060-150697582 | Common:8; Rare:436 |