Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:71080945-71081364 | Rare:112 | ||||
chr1:74198148-74198293 | Common:1; Rare:80 | ||||
chr1:74733001-74733266 | Common:5; Rare:85 | ||||
chr1:77219400-77219482 | Rare:38 | ||||
chr1:77888429-77888758 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77941847-77942197 | Rare:114; Clinvar:12; Clinvar (benign):5 | ||||
chr1:77979000-77979233 | Common:2; Rare:90 | ||||
chr1:78004552-78004960 | Common:4; Rare:93 | ||||
chr1:84077864-84078230 | Common:1; Rare:125 | ||||
chr1:84479202-84479309 | Common:3; Rare:53 | ||||
chr1:84573954-84574114 | Common:1; Rare:29 | ||||
chr1:84574388-84574578 | Common:1; Rare:59 | ||||
chr1:85259629-85259892 | Common:4; Rare:91 | ||||
chr1:85276114-85276306 | Common:3; Rare:47 | ||||
chr1:85276469-85276774 | Common:5; Rare:90 |