Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:138331783-138332122 | Common:2; Rare:83 | ||||
chr5:138543095-138543440 | Common:2; Rare:102 | ||||
chr5:138753268-138753491 | Common:2; Rare:76 | ||||
chr5:139198288-139198526 | Rare:80; Clinvar (benign):1 | ||||
chr5:139273975-139274133 | Rare:73 | ||||
chr5:139293532-139293805 | Rare:89 | ||||
chr5:139439453-139439646 | Common:2; Rare:52 | ||||
chr5:139561112-139561397 | Common:1; Rare:113 | ||||
chr5:139561645-139561794 | Rare:56 | ||||
chr5:140303065-140303160 | Common:1; Rare:28 | ||||
chr5:140557426-140557519 | Rare:53 | ||||
chr5:140564556-140564837 | Rare:74 | ||||
chr5:140647591-140647898 | Common:5; Rare:124; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691313-140691633 | Common:1; Rare:111; Clinvar:8; Clinvar (benign):1 | ||||
chr5:141320742-141320886 | Common:1; Rare:44 |