Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:132866334-132866709 | Common:2; Rare:118; Clinvar:1; Clinvar (benign):1 | ||||
chr5:133051862-133052125 | Rare:96 | ||||
chr5:133968573-133968696 | Rare:57 | ||||
chr5:134004654-134004855 | Common:1; Rare:75 | ||||
chr5:134226033-134226389 | Common:1; Rare:115 | ||||
chr5:134648721-134648816 | Rare:21 | ||||
chr5:138178621-138179178 | Common:3; Rare:114 | ||||
chr5:138543112-138543441 | Common:2; Rare:101 | ||||
chr5:138753283-138753488 | Common:2; Rare:67 | ||||
chr5:140564560-140564837 | Rare:74 | ||||
chr5:140647594-140647883 | Common:5; Rare:116; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691325-140691641 | Common:1; Rare:106; Clinvar:8; Clinvar (benign):1 | ||||
chr5:141320762-141320912 | Common:1; Rare:47 | ||||
chr5:141636810-141637001 | Common:2; Rare:83 | ||||
chr5:144170592-144170852 | Common:2; Rare:81 |