Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:138178946-138179160 | Common:2; Rare:45 | ||||
chr5:138465815-138465861 | Rare:14 | ||||
chr5:138543095-138543558 | Common:2; Rare:150 | ||||
chr5:138753280-138753499 | Common:2; Rare:73 | ||||
chr5:139198289-139198526 | Rare:80; Clinvar (benign):1 | ||||
chr5:139404056-139404302 | Rare:75 | ||||
chr5:139439453-139439637 | Common:2; Rare:50 | ||||
chr5:139561733-139561793 | Rare:27 | ||||
chr5:140174867-140175253 | Rare:113 | ||||
chr5:140303048-140303115 | Common:1; Rare:26 | ||||
chr5:140557426-140557530 | Common:1; Rare:61 | ||||
chr5:140564676-140564837 | Rare:48 | ||||
chr5:140647585-140647883 | Common:5; Rare:122; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691318-140691497 | Common:1; Rare:65; Clinvar:7 | ||||
chr5:141320732-141320890 | Common:2; Rare:49 |