Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235882459-235882537 | Common:1; Rare:11 | ||||
chr1:235917456-235917812 | Common:2; Rare:63 | ||||
chr1:235919170-235919329 | Common:3; Rare:28 | ||||
chr1:235971841-235971999 | Common:1; Rare:44 | ||||
chr1:238485015-238485243 | Common:4; Rare:53 | ||||
chr1:240338965-240339128 | Common:4; Rare:46 | ||||
chr1:240405926-240406087 | Common:9; Rare:33 | ||||
chr1:240406277-240406448 | Rare:26 | ||||
chr1:243201364-243201627 | Common:1; Rare:42 | ||||
chr1:244451107-244451244 | Common:2; Rare:37 | ||||
chr1:244863754-244863875 | Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
chr1:244970956-244971138 | Rare:57 | ||||
chr1:245216980-245217046 | Rare:14 | ||||
chr1:245513110-245513264 | Common:6; Rare:28 | ||||
chr1:246067726-246067932 | Common:3; Rare:46 |