Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:67053140-67053608 | Common:3; Rare:103 | ||||
chr1:67053611-67054273 | Common:6; Rare:255; Clinvar (pathogenic):1 | ||||
chr1:67054316-67054456 | Common:3; Rare:32 | ||||
chr1:67429130-67429240 | Rare:19 | ||||
chr1:67429639-67429917 | Common:1; Rare:72 | ||||
chr1:67430301-67430715 | Rare:156 | ||||
chr1:67430783-67430992 | Common:1; Rare:63 | ||||
chr1:67684904-67685537 | Common:3; Rare:188 | ||||
chr1:67685776-67686108 | Common:1; Rare:103 | ||||
chr1:67832757-67832942 | Common:1; Rare:48 | ||||
chr1:67832948-67833264 | Common:1; Rare:71 | ||||
chr1:67833303-67833632 | Common:4; Rare:110 | ||||
chr1:67833645-67833732 | Common:1; Rare:29 | ||||
chr1:67833755-67833836 | Rare:24 | ||||
chr1:68231246-68231283 | Rare:11 |