Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70221306-70221500 | Rare:84 | ||||
chr1:70354676-70354838 | Rare:58 | ||||
chr1:70411069-70411297 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080996-71081353 | Rare:97 | ||||
chr1:74733030-74733266 | Common:5; Rare:77 | ||||
chr1:75724658-75724778 | Common:1; Rare:59; Clinvar:4; Clinvar (benign):1 | ||||
chr1:77219400-77219498 | Rare:45 | ||||
chr1:77683369-77683648 | Common:1; Rare:87 | ||||
chr1:77888461-77888528 | Rare:17 | ||||
chr1:77979022-77979302 | Common:2; Rare:92 | ||||
chr1:81800061-81800379 | Common:2; Rare:83 | ||||
chr1:84077904-84078171 | Common:1; Rare:95 | ||||
chr1:84690425-84690688 | Rare:82 | ||||
chr1:85276432-85276570 | Common:2; Rare:42 | ||||
chr1:85276609-85276682 | Common:1; Rare:18 |