Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:135399095-135399435 | Rare:84 | ||||
chr5:135578978-135579144 | Common:2; Rare:44 | ||||
chr5:136029066-136029188 | Rare:40 | ||||
chr5:138178941-138179181 | Common:3; Rare:50 | ||||
chr5:138543121-138543441 | Common:2; Rare:99 | ||||
chr5:139561696-139561794 | Rare:40 | ||||
chr5:140303065-140303171 | Common:1; Rare:30 | ||||
chr5:140564546-140564837 | Rare:76 | ||||
chr5:140647603-140647900 | Common:5; Rare:120; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691322-140691497 | Common:1; Rare:62; Clinvar:7 | ||||
chr5:141636825-141637023 | Common:1; Rare:75 | ||||
chr5:141923691-141923909 | Common:1; Rare:67 | ||||
chr5:142324992-142325212 | Rare:73 | ||||
chr5:146182575-146182916 | Common:4; Rare:104 | ||||
chr5:147510007-147510273 | Common:1; Rare:44 |