Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:7636983-7637152 | Common:2; Rare:51; Clinvar (benign):1 | ||||
chr19:7903542-7903941 | Rare:133 | ||||
chr19:7920188-7920393 | Rare:83 | ||||
chr19:7925480-7925759 | Common:2; Rare:74 | ||||
chr19:7926603-7926643 | Rare:5 | ||||
chr19:7943625-7943990 | Rare:102 | ||||
chr19:8005498-8005822 | Common:1; Rare:114 | ||||
chr19:8308291-8308665 | Common:3; Rare:120 | ||||
chr19:8321308-8321703 | Common:2; Rare:159 | ||||
chr19:8363959-8364167 | Common:1; Rare:52 | ||||
chr19:8390048-8390456 | Common:2; Rare:115 | ||||
chr19:8444791-8445008 | Common:4; Rare:93 | ||||
chr19:9140311-9140456 | Common:1; Rare:43 | ||||
chr19:9435495-9435608 | Rare:47 | ||||
chr19:9538574-9538741 | Common:1; Rare:52 |