Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:69568202-69568343 | Rare:48 | ||||
chr1:70205542-70205761 | Rare:70 | ||||
chr1:70221306-70221530 | Rare:98 | ||||
chr1:70354659-70354862 | Rare:67 | ||||
chr1:71080984-71081394 | Rare:114 | ||||
chr1:74198148-74198340 | Common:2; Rare:108 | ||||
chr1:74733030-74733259 | Common:5; Rare:73 | ||||
chr1:75724308-75724773 | Common:6; Rare:162; Clinvar:7; Clinvar (benign):5 | ||||
chr1:76074539-76074772 | Common:2; Rare:88 | ||||
chr1:77219375-77219498 | Rare:62 | ||||
chr1:77682641-77682712 | Rare:17 | ||||
chr1:77683322-77683532 | Common:1; Rare:71 | ||||
chr1:77888429-77888710 | Common:1; Rare:62; Clinvar:2 | ||||
chr1:77979000-77979298 | Common:2; Rare:107 | ||||
chr1:78004552-78004882 | Common:3; Rare:81 |