Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:158177815-158178059 | Common:4; Rare:55 | ||||
chr1:159790315-159790715 | Common:5; Rare:174 | ||||
chr1:159867770-159868070 | Common:3; Rare:61 | ||||
chr1:159900960-159901470 | Common:2; Rare:90 | ||||
chr1:159913650-159913950 | Common:4; Rare:51 | ||||
chr1:159913900-159914160 | Common:3; Rare:48 | ||||
chr1:159959532-159959771 | Rare:35 | ||||
chr1:159991477-159991877 | Common:1; Rare:149 | ||||
chr1:160030718-160031118 | Rare:201; Clinvar:1; Clinvar (benign):2 | ||||
chr1:160344189-160344331 | Rare:20 | ||||
chr1:160407920-160408490 | Common:3; Rare:109 | ||||
chr1:160781340-160781760 | Common:2; Rare:94 | ||||
chr1:160989853-160990706 | Common:9; Rare:221 | ||||
chr1:161013741-161014002 | Common:1; Rare:49 | ||||
chr1:161020039-161020439 | Common:3; Rare:178 |