Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37859586-37859764 | Common:3; Rare:58 | ||||
chr1:37989981-37990105 | Rare:47 | ||||
chr1:38005495-38005766 | Common:1; Rare:68 | ||||
chr1:38012443-38012799 | Common:1; Rare:106 | ||||
chr1:38859692-38859940 | Rare:95 | ||||
chr1:38873306-38873551 | Common:3; Rare:84 | ||||
chr1:39026237-39026398 | Common:1; Rare:43 | ||||
chr1:39883447-39883570 | Common:1; Rare:51; Clinvar (pathogenic):1 | ||||
chr1:39955004-39955193 | Common:1; Rare:50 | ||||
chr1:40040089-40040240 | Common:1; Rare:27 | ||||
chr1:40040419-40040799 | Common:3; Rare:120 | ||||
chr1:40161231-40161402 | Common:1; Rare:47 | ||||
chr1:40257908-40258292 | Common:4; Rare:106; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40508674-40508773 | Common:3; Rare:27 | ||||
chr1:40691495-40691810 | Common:3; Rare:155 |