Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49580536-49580632 | Rare:34 | ||||
chr19:49690973-49691144 | Common:1; Rare:38 | ||||
chr19:49800920-49801012 | Rare:23 | ||||
chr19:49877383-49877717 | Common:1; Rare:85 | ||||
chr19:49929404-49929567 | Common:4; Rare:59 | ||||
chr19:49929923-49930219 | Common:1; Rare:70 | ||||
chr19:50384028-50384377 | Common:2; Rare:147; Clinvar:1; Clinvar (benign):2 | ||||
chr19:50476275-50476542 | Rare:121 | ||||
chr19:51311578-51311884 | Common:4; Rare:63 | ||||
chr19:51366339-51366505 | Common:5; Rare:44; Clinvar (benign):2 | ||||
chr19:51887866-51888059 | Rare:69 | ||||
chr19:52008160-52008359 | Rare:61 | ||||
chr19:52028336-52028462 | Common:3; Rare:26 | ||||
chr19:52139875-52140174 | Common:3; Rare:81 | ||||
chr19:52171441-52171764 | Common:3; Rare:81 |