Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:1801286-1801460 | Common:4; Rare:87; Clinvar:3; Clinvar (benign):1 | ||||
chr5:6632990-6633318 | Common:6; Rare:103; Clinvar:8; Clinvar (benign):3 | ||||
chr5:7868987-7869204 | Common:2; Rare:112; Clinvar (benign):1 | ||||
chr5:10249869-10250427 | Common:19; Rare:260; Clinvar:5; Clinvar (benign):2 | ||||
chr5:10353590-10353901 | Common:3; Rare:116 | ||||
chr5:10441803-10441939 | Rare:39 | ||||
chr5:16465566-16465894 | Rare:85 | ||||
chr5:31532026-31532367 | Common:3; Rare:98 | ||||
chr5:32174277-32174395 | Common:1; Rare:43 | ||||
chr5:33440606-33441125 | Common:7; Rare:144 | ||||
chr5:34008027-34008263 | Common:2; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
chr5:34656158-34656473 | Common:3; Rare:80 | ||||
chr5:34686781-34686884 | Common:1; Rare:15 | ||||
chr5:34915218-34915355 | Rare:38 | ||||
chr5:34915468-34915755 | Common:1; Rare:76 |