Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:47176055-47176257 | Common:2; Rare:70 | ||||
chr2:47176387-47176605 | Rare:148; Clinvar (benign):5 | ||||
chr2:47345047-47345181 | Rare:36 | ||||
chr2:47369035-47369584 | Common:5; Rare:230; Clinvar:18; Clinvar (benign):6 | ||||
chr2:47402890-47402908 | Rare:8; Clinvar:3; Clinvar (benign):1 | ||||
chr2:47402945-47403403 | Common:1; Rare:229; Clinvar:90; Clinvar (benign):59; Clinvar (pathogenic):8 | ||||
chr2:47570066-47570159 | Rare:24 | ||||
chr2:47570909-47571026 | Rare:37 | ||||
chr2:47695961-47695984 | Rare:4 | ||||
chr2:47782886-47783269 | Common:3; Rare:174; Clinvar:14; Clinvar (benign):24; Clinvar (pathogenic):2 | ||||
chr2:47783344-47783457 | Common:2; Rare:38; Clinvar:18; Clinvar (benign):15 | ||||
chr2:47783458-47783681 | Common:1; Rare:77; Clinvar:7; Clinvar (benign):8 | ||||
chr2:47783761-47784046 | Common:6; Rare:65; Clinvar (benign):1 | ||||
chr2:47905491-47905867 | Common:3; Rare:184 | ||||
chr2:48314183-48314367 | Common:1; Rare:59 |