Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:3385536-3385712 | Rare:38 | ||||
chr4:4248178-4248311 | Common:4; Rare:55 | ||||
chr4:4290118-4290245 | Common:1; Rare:47 | ||||
chr4:4541972-4542142 | Common:1; Rare:70 | ||||
chr4:5019478-5019568 | Rare:21 | ||||
chr4:6640543-6640716 | Common:2; Rare:70 | ||||
chr4:6987014-6987291 | Common:2; Rare:86 | ||||
chr4:7068034-7068373 | Common:5; Rare:116 | ||||
chr4:15681474-15681879 | Common:4; Rare:140 | ||||
chr4:15703208-15703230 | Rare:8 | ||||
chr4:17614581-17614653 | Common:1; Rare:32 | ||||
chr4:17810681-17811020 | Common:3; Rare:104 | ||||
chr4:25160405-25160732 | Common:3; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
chr4:25233841-25234074 | Rare:98 | ||||
chr4:25914051-25914275 | Common:2; Rare:98 |