Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:26860497-26861036 | Common:3; Rare:148 | ||||
chr10:27099959-27100063 | Rare:22 | ||||
chr10:27100152-27100272 | Common:1; Rare:67; Clinvar:5; Clinvar (benign):2 | ||||
chr10:27100366-27100674 | Common:5; Rare:80; Clinvar:4; Clinvar (benign):3 | ||||
chr10:27153869-27153973 | Common:2; Rare:24 | ||||
chr10:27153976-27154051 | Rare:19 | ||||
chr10:27154240-27154528 | Rare:81 | ||||
chr10:27154885-27155058 | Common:1; Rare:37; Clinvar (benign):1 | ||||
chr10:27155078-27155116 | Rare:10; Clinvar:2 | ||||
chr10:27155120-27155478 | Common:7; Rare:138; Clinvar:5; Clinvar (benign):8 | ||||
chr10:27155812-27156190 | Common:7; Rare:80 | ||||
chr10:27240316-27240451 | Rare:41 | ||||
chr10:27240458-27240942 | Common:3; Rare:133 | ||||
chr10:27241840-27241877 | Rare:9 | ||||
chr10:27241884-27242347 | Common:3; Rare:161 |