Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:924860-925120 | Common:2; Rare:69 | ||||
chr1:959241-959463 | Common:1; Rare:107 | ||||
chr1:1000051-1000519 | Common:8; Rare:155 | ||||
chr1:1000703-1000964 | Common:3; Rare:71 | ||||
chr1:1001180-1001490 | Common:3; Rare:64 | ||||
chr1:1013323-1013505 | Common:3; Rare:59 | ||||
chr1:1019653-1019755 | Common:1; Rare:27 | ||||
chr1:1019930-1020121 | Common:1; Rare:66 | ||||
chr1:1115360-1116700 | Common:10; Rare:514 | ||||
chr1:1231482-1231636 | Common:1; Rare:47 | ||||
chr1:1231909-1232287 | Rare:137; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:1273819-1274079 | Common:1; Rare:95 | ||||
chr1:1304650-1305000 | Common:2; Rare:100 | ||||
chr1:1305558-1305958 | Common:3; Rare:168 | ||||
chr1:1307810-1308220 | Common:1; Rare:104 |