Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58002696-58002929 | Common:3; Rare:127 | ||||
chr19:58228830-58228949 | Common:1; Rare:46 | ||||
chr19:58278736-58278987 | Common:2; Rare:79 | ||||
chr19:58326875-58326994 | Common:1; Rare:28 | ||||
chr19:58347620-58347780 | Common:8; Rare:77 | ||||
chr19:58558538-58558725 | Rare:52 | ||||
chr2:3377798-3377931 | Rare:34 | ||||
chr2:3558251-3558509 | Common:5; Rare:113 | ||||
chr2:3575127-3575358 | Common:2; Rare:66; Clinvar:3; Clinvar (benign):5 | ||||
chr2:9423447-9423682 | Rare:76 | ||||
chr2:10302751-10302994 | Common:4; Rare:68 | ||||
chr2:10448314-10448682 | Common:1; Rare:108 | ||||
chr2:17753725-17753910 | Common:2; Rare:68 | ||||
chr2:20051564-20051874 | Common:1; Rare:79 | ||||
chr2:24076335-24076434 | Rare:34 |