Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:217630754-217631475 | Common:6; Rare:216 | ||||
chr1:217631689-217631901 | Common:1; Rare:33 | ||||
chr1:218284922-218285414 | Common:6; Rare:170 | ||||
chr1:218285546-218285589 | Common:1; Rare:7 | ||||
chr1:218345493-218346042 | Common:4; Rare:130; Clinvar:6; Clinvar (benign):4 | ||||
chr1:218346105-218346384 | Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
chr1:218347343-218347369 | Rare:4 | ||||
chr1:219173684-219173954 | Common:2; Rare:125 | ||||
chr1:219174110-219174237 | Rare:21 | ||||
chr1:219174245-219174301 | Rare:12 | ||||
chr1:219174601-219174928 | Rare:68 | ||||
chr1:220046017-220046173 | Common:1; Rare:39 | ||||
chr1:220046199-220046840 | Common:1; Rare:178 | ||||
chr1:220089654-220090019 | Common:2; Rare:78 | ||||
chr1:220090172-220090365 | Common:2; Rare:24 |