Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:67684929-67685208 | Common:2; Rare:74 | ||||
chr1:67685792-67686113 | Common:1; Rare:101 | ||||
chr1:67833332-67833529 | Common:2; Rare:78 | ||||
chr1:68232476-68232673 | Rare:43 | ||||
chr1:70205504-70205770 | Rare:96 | ||||
chr1:70221296-70221530 | Rare:102 | ||||
chr1:70354634-70354851 | Rare:72 | ||||
chr1:70411069-70411291 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080956-71081373 | Rare:110 | ||||
chr1:72282663-72282973 | Common:4; Rare:90 | ||||
chr1:74198141-74198340 | Common:2; Rare:112 | ||||
chr1:74732994-74733459 | Common:6; Rare:168 | ||||
chr1:75724358-75724773 | Common:5; Rare:149; Clinvar:7; Clinvar (benign):5 | ||||
chr1:76074572-76074880 | Common:2; Rare:100 | ||||
chr1:77219389-77219520 | Rare:59 |