Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20486179-20486379 | Rare:47 | ||||
chr1:20508079-20508229 | Common:2; Rare:54 | ||||
chr1:20589025-20589143 | Common:4; Rare:42 | ||||
chr1:20661346-20661687 | Common:3; Rare:123; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786596-20786870 | Rare:103 | ||||
chr1:20787219-20787447 | Rare:107 | ||||
chr1:21176883-21177069 | Rare:38 | ||||
chr1:21290203-21290499 | Common:1; Rare:64 | ||||
chr1:21440009-21440207 | Common:2; Rare:46 | ||||
chr1:21783005-21783283 | Common:2; Rare:97 | ||||
chr1:22451644-22451888 | Common:1; Rare:76 | ||||
chr1:23344219-23344417 | Common:2; Rare:78 | ||||
chr1:23344651-23344831 | Common:1; Rare:66 | ||||
chr1:23368214-23368488 | Common:1; Rare:81 | ||||
chr1:23559427-23559671 | Common:2; Rare:106 |