Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25338214-25338447 | Common:1; Rare:80 | ||||
chr1:25819914-25820013 | Common:1; Rare:28 | ||||
chr1:25859351-25859609 | Common:3; Rare:110 | ||||
chr1:26279947-26280158 | Rare:123 | ||||
chr1:26432104-26432403 | Common:5; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26921554-26921825 | Common:3; Rare:85 | ||||
chr1:27490049-27490324 | Rare:92 | ||||
chr1:27725760-27725985 | Common:2; Rare:56 | ||||
chr1:28505828-28506056 | Common:2; Rare:93 | ||||
chr1:28643020-28643231 | Rare:82 | ||||
chr1:28668645-28668826 | Common:1; Rare:59 | ||||
chr1:28736713-28737049 | Common:3; Rare:111 | ||||
chr1:29181784-29182147 | Common:3; Rare:143 | ||||
chr1:29230882-29231115 | Rare:80; Clinvar:1 | ||||
chr1:31065658-31065932 | Common:1; Rare:97 |