Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150162825-150162975 | Common:2; Rare:40 | ||||
chr1:150163131-150163405 | Common:3; Rare:67 | ||||
chr1:150163764-150164164 | Common:6; Rare:79 | ||||
chr1:150173283-150173594 | Common:3; Rare:51 | ||||
chr1:150213541-150213856 | Common:3; Rare:76 | ||||
chr1:150256037-150256161 | Common:1; Rare:28 | ||||
chr1:150259850-150260190 | Common:1; Rare:84 | ||||
chr1:150281030-150281890 | Common:2; Rare:226 | ||||
chr1:150515487-150515788 | Rare:87 | ||||
chr1:150543643-150544094 | Common:1; Rare:149 | ||||
chr1:150560900-150561230 | Common:1; Rare:62; Clinvar (benign):1 | ||||
chr1:150561459-150561626 | Rare:41 | ||||
chr1:150567804-150567941 | Rare:38 | ||||
chr1:150568160-150568520 | Rare:78 | ||||
chr1:151060278-151060487 | Rare:39 |