Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:51345076-51345530 | Common:4; Rare:196; Clinvar:6; Clinvar (benign):6 | ||||
chr19:51394170-51394600 | Common:10; Rare:163 | ||||
chr19:51594270-51594680 | Common:6; Rare:162 | ||||
chr19:51687690-51688450 | Common:9; Rare:221 | ||||
chr19:51688950-51689400 | Common:19; Rare:215 | ||||
chr19:52922931-52923801 | Common:23; Rare:451 | ||||
chr19:52942540-52942805 | Common:8; Rare:96 | ||||
chr19:53889620-53889920 | Common:1; Rare:118; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):18 | ||||
chr19:53961820-53962340 | Common:6; Rare:117 | ||||
chr19:53980190-53980730 | Common:7; Rare:215 | ||||
chr19:55189210-55189820 | Common:7; Rare:244 | ||||
chr19:55215750-55216180 | Common:7; Rare:135 | ||||
chr19:55216380-55216830 | Common:6; Rare:145 | ||||
chr19:55216852-55217252 | Rare:100 | ||||
chr19:55472530-55472760 | Common:6; Rare:90 |