Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:72282669-72282974 | Common:4; Rare:89 | ||||
chr1:74198145-74198340 | Common:2; Rare:110 | ||||
chr1:74732994-74733360 | Common:6; Rare:129 | ||||
chr1:75724315-75724803 | Common:6; Rare:172; Clinvar:7; Clinvar (benign):5 | ||||
chr1:76074570-76074864 | Common:2; Rare:94 | ||||
chr1:77219391-77219520 | Rare:59 | ||||
chr1:77888191-77888388 | Common:1; Rare:43 | ||||
chr1:77888451-77888758 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77947166-77947268 | Rare:22 | ||||
chr1:77948899-77948961 | Common:1; Rare:10 | ||||
chr1:77978887-77979298 | Common:3; Rare:147 | ||||
chr1:77979456-77979536 | Common:1; Rare:21 | ||||
chr1:78004547-78004960 | Common:4; Rare:96 | ||||
chr1:78045718-78046078 | Rare:87 | ||||
chr1:78490883-78491048 | Common:1; Rare:32 |