Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32394410-32394690 | Common:1; Rare:77 | ||||
chr1:32539308-32539434 | Rare:25 | ||||
chr1:32650933-32651309 | Common:2; Rare:145 | ||||
chr1:32817240-32817689 | Common:1; Rare:120; Clinvar:5; Clinvar (benign):2 | ||||
chr1:33021443-33021656 | Rare:50; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:33080994-33081165 | Common:1; Rare:43 | ||||
chr1:34782198-34782349 | Rare:22 | ||||
chr1:34792907-34793013 | Rare:27 | ||||
chr1:35192390-35192693 | Common:2; Rare:88 | ||||
chr1:35193092-35193440 | Common:2; Rare:117 | ||||
chr1:35557629-35557863 | Common:2; Rare:93 | ||||
chr1:35641480-35641639 | Common:1; Rare:36 | ||||
chr1:35930940-35931110 | Common:2; Rare:60 | ||||
chr1:36306897-36307138 | Common:1; Rare:100 | ||||
chr1:37474363-37474587 | Common:1; Rare:88 |