Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:959193-959450 | Common:1; Rare:136 | ||||
chr1:960512-960668 | Rare:44 | ||||
chr1:966928-967123 | Rare:84 | ||||
chr1:1000064-1000540 | Common:8; Rare:160 | ||||
chr1:1000694-1000871 | Common:3; Rare:50 | ||||
chr1:1013309-1013584 | Common:5; Rare:85 | ||||
chr1:1019898-1020188 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
chr1:1231485-1231606 | Common:1; Rare:37 | ||||
chr1:1231884-1232330 | Rare:162; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:1273778-1274144 | Common:3; Rare:133 | ||||
chr1:1305651-1305855 | Rare:69 | ||||
chr1:1308306-1308671 | Common:8; Rare:152 | ||||
chr1:1324576-1324884 | Common:3; Rare:157 | ||||
chr1:1349338-1349561 | Common:2; Rare:75 | ||||
chr1:1349713-1349873 | Common:1; Rare:50 |