Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:959217-959391 | Common:1; Rare:106 | ||||
chr1:960530-960666 | Rare:37 | ||||
chr1:999943-1000556 | Common:10; Rare:209 | ||||
chr1:1000844-1001012 | Rare:44 | ||||
chr1:1013382-1013575 | Common:4; Rare:62 | ||||
chr1:1020209-1020331 | Common:2; Rare:39; Clinvar:3; Clinvar (benign):1 | ||||
chr1:1221274-1221577 | Common:1; Rare:93 | ||||
chr1:1231887-1232279 | Rare:139; Clinvar (benign):2 | ||||
chr1:1232725-1232927 | Common:1; Rare:95; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr1:1273768-1274045 | Common:1; Rare:109 | ||||
chr1:1307874-1308170 | Rare:76 | ||||
chr1:1308333-1308699 | Common:9; Rare:157 | ||||
chr1:1315514-1315859 | Common:6; Rare:105 | ||||
chr1:1324579-1324863 | Common:3; Rare:148 | ||||
chr1:1349378-1349571 | Common:2; Rare:64 |