Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:75791201-75791351 | Rare:30 | ||||
chr1:76074570-76074883 | Common:2; Rare:101 | ||||
chr1:77219356-77219547 | Rare:87 | ||||
chr1:77281799-77282081 | Common:4; Rare:89 | ||||
chr1:77682606-77682723 | Rare:30 | ||||
chr1:77683261-77683483 | Rare:63 | ||||
chr1:77759646-77759965 | Common:3; Rare:127 | ||||
chr1:77779536-77779912 | Rare:117 | ||||
chr1:77888078-77888756 | Common:3; Rare:157; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77918024-77918112 | Rare:25; Clinvar (benign):3 | ||||
chr1:77945929-77946112 | Rare:31 | ||||
chr1:77946322-77946864 | Rare:84 | ||||
chr1:77947608-77947984 | Rare:72 | ||||
chr1:77978773-77978858 | Rare:25 | ||||
chr1:77978870-77979344 | Common:4; Rare:165 |