Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:56387164-56387244 | Rare:20 | ||||
chr4:56387409-56387547 | Rare:48 | ||||
chr4:56435467-56435973 | Common:6; Rare:166 | ||||
chr4:56436040-56436315 | Rare:101 | ||||
chr4:56467515-56467915 | Common:3; Rare:146; Clinvar (benign):5 | ||||
chr4:56977541-56977785 | Common:2; Rare:92 | ||||
chr4:61200605-61200965 | Common:4; Rare:96 | ||||
chr4:61201173-61201238 | Rare:20 | ||||
chr4:61201245-61201390 | Common:2; Rare:48 | ||||
chr4:61201894-61202136 | Rare:54 | ||||
chr4:65669486-65669612 | Common:1; Rare:33 | ||||
chr4:65670280-65670635 | Common:2; Rare:96 | ||||
chr4:67545364-67545763 | Common:2; Rare:96 | ||||
chr4:67701064-67701419 | Common:4; Rare:165 | ||||
chr4:68349731-68350214 | Common:2; Rare:172 |