Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:7636973-7637152 | Common:2; Rare:55; Clinvar (benign):1 | ||||
chr19:7702109-7702320 | Common:2; Rare:42 | ||||
chr19:7903501-7903941 | Common:2; Rare:148 | ||||
chr19:7920187-7920486 | Rare:113 | ||||
chr19:7943632-7943988 | Rare:100 | ||||
chr19:8005508-8005822 | Common:1; Rare:110 | ||||
chr19:8320855-8321159 | Rare:86 | ||||
chr19:8321308-8321703 | Common:2; Rare:159 | ||||
chr19:8364045-8364183 | Common:2; Rare:37 | ||||
chr19:8390032-8390453 | Common:2; Rare:118 | ||||
chr19:8444800-8445109 | Common:3; Rare:139; Clinvar (benign):1 | ||||
chr19:8514138-8514229 | Common:1; Rare:28 | ||||
chr19:8526342-8526468 | Common:1; Rare:40 | ||||
chr19:8577422-8577533 | Common:2; Rare:23 | ||||
chr19:8832207-8832353 | Common:1; Rare:54 |