Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:74732994-74733481 | Common:10; Rare:248 | ||||
chr1:75724110-75724440 | Common:8; Rare:172; Clinvar:2; Clinvar (benign):4 | ||||
chr1:75724598-75724805 | Common:4; Rare:174; Clinvar:9; Clinvar (benign):4 | ||||
chr1:75785801-75786392 | Common:10; Rare:346 | ||||
chr1:77219368-77219536 | Rare:127 | ||||
chr1:77682536-77682720 | Rare:44 | ||||
chr1:77683292-77683652 | Common:2; Rare:180 | ||||
chr1:77683780-77684110 | Rare:85 | ||||
chr1:77759665-77759973 | Common:6; Rare:232 | ||||
chr1:77779536-77779855 | Rare:141 | ||||
chr1:77978998-77979414 | Common:6; Rare:204 | ||||
chr1:77979410-77979700 | Common:1; Rare:93 | ||||
chr1:78004547-78004951 | Common:8; Rare:185 | ||||
chr1:83999101-83999448 | Common:6; Rare:102 | ||||
chr1:84077810-84078222 | Common:4; Rare:248 |