Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:46297650-46297827 | Rare:67; Clinvar:5; Clinvar (benign):1 | ||||
chr2:46375420-46375835 | Common:2; Rare:116 | ||||
chr2:46541501-46541842 | Common:1; Rare:71 | ||||
chr2:46543130-46543473 | Rare:88 | ||||
chr2:46617012-46617270 | Common:7; Rare:115 | ||||
chr2:46915721-46915944 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
chr2:46916007-46916188 | Common:2; Rare:56 | ||||
chr2:46941677-46941792 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
chr2:47176439-47176764 | Common:4; Rare:159; Clinvar (benign):5 | ||||
chr2:47345075-47345161 | Rare:22 | ||||
chr2:47369151-47369577 | Common:4; Rare:182; Clinvar:17; Clinvar (benign):6 | ||||
chr2:47402951-47403194 | Common:1; Rare:111; Clinvar:36; Clinvar (benign):26 | ||||
chr2:47782956-47783199 | Common:2; Rare:108; Clinvar:4; Clinvar (benign):7 | ||||
chr2:47905330-47905824 | Common:5; Rare:221 | ||||
chr2:48314602-48315055 | Common:1; Rare:184 |