Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93180110-93180695 | Common:1; Rare:220 | ||||
chr1:93345788-93345946 | Common:3; Rare:61 | ||||
chr1:93847204-93847315 | Common:1; Rare:29 | ||||
chr1:93879144-93879274 | Common:1; Rare:44 | ||||
chr1:94237552-94237748 | Rare:76 | ||||
chr1:94418182-94418470 | Common:2; Rare:105 | ||||
chr1:94541612-94541991 | Common:1; Rare:112 | ||||
chr1:94820190-94820410 | Common:3; Rare:61 | ||||
chr1:94903141-94903444 | Common:1; Rare:60 | ||||
chr1:94926842-94926909 | Rare:16 | ||||
chr1:94926947-94927456 | Common:4; Rare:161 | ||||
chr1:95072876-95073018 | Rare:55 | ||||
chr1:95233910-95234243 | Common:5; Rare:103 | ||||
chr1:98661598-98661869 | Common:2; Rare:96 | ||||
chr1:99850247-99850647 | Rare:84; Clinvar:3; Clinvar (benign):2 |