Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161132587-161132680 | Common:1; Rare:34 | ||||
chr1:161159392-161159507 | Common:1; Rare:29 | ||||
chr1:161166271-161166511 | Common:2; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161199053-161199320 | Rare:43 | ||||
chr1:161225768-161226063 | Common:10; Rare:43 | ||||
chr1:161314305-161314405 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):2 | ||||
chr1:161766136-161766363 | Common:3; Rare:65 | ||||
chr1:162497755-162497849 | Common:1; Rare:29 | ||||
chr1:162790527-162790781 | Common:4; Rare:75 | ||||
chr1:163321723-163322057 | Common:1; Rare:91 | ||||
chr1:164559300-164559442 | Rare:42 | ||||
chr1:164559522-164559800 | Common:2; Rare:66 | ||||
chr1:165698524-165698634 | Common:2; Rare:64 | ||||
chr1:165768747-165768938 | Common:1; Rare:77 | ||||
chr1:166839348-166839522 | Rare:51 |