Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:212035529-212035748 | Common:1; Rare:54 | ||||
chr1:212285050-212285457 | Common:3; Rare:133 | ||||
chr1:212608512-212608761 | Rare:64 | ||||
chr1:212791756-212791926 | Common:3; Rare:68 | ||||
chr1:212858066-212858283 | Common:3; Rare:56; Clinvar:1 | ||||
chr1:213987699-213987973 | Rare:51 | ||||
chr1:214281005-214281257 | Common:2; Rare:109 | ||||
chr1:215567447-215567682 | Rare:75 | ||||
chr1:217076932-217077106 | Common:2; Rare:33 | ||||
chr1:217630994-217631381 | Common:2; Rare:114 | ||||
chr1:218346872-218346932 | Rare:16; Clinvar:4; Clinvar (pathogenic):1 | ||||
chr1:219173780-219173900 | Common:1; Rare:65 | ||||
chr1:221742047-221742288 | Rare:61 | ||||
chr1:222589912-222590184 | Rare:56 | ||||
chr1:222644127-222644388 | Common:2; Rare:76 |