Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:65148905-65149051 | Common:1; Rare:46 | ||||
chr1:66332127-66332364 | Rare:45 | ||||
chr1:66924800-66925031 | Rare:100 | ||||
chr1:66925149-66925518 | Common:2; Rare:116 | ||||
chr1:67053619-67053776 | Common:4; Rare:62 | ||||
chr1:67429989-67430449 | Rare:177 | ||||
chr1:67833332-67833527 | Common:2; Rare:77 | ||||
chr1:68232455-68232643 | Rare:43 | ||||
chr1:70205542-70205775 | Rare:73 | ||||
chr1:70354699-70354844 | Rare:52 | ||||
chr1:71080948-71081392 | Rare:122 | ||||
chr1:72282669-72282974 | Common:4; Rare:89 | ||||
chr1:74198148-74198347 | Common:2; Rare:111 | ||||
chr1:74732966-74733305 | Common:6; Rare:114 | ||||
chr1:75724308-75724598 | Common:4; Rare:72; Clinvar:2; Clinvar (benign):3 |