Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25247449-25247630 | Common:2; Rare:63 | ||||
chr1:25338215-25338408 | Common:1; Rare:65 | ||||
chr1:25819866-25820193 | Common:4; Rare:102 | ||||
chr1:26432123-26432392 | Common:4; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26900441-26900505 | Rare:25 | ||||
chr1:26921517-26921830 | Common:3; Rare:99 | ||||
chr1:27725760-27725998 | Common:2; Rare:63 | ||||
chr1:28505746-28506050 | Common:4; Rare:109 | ||||
chr1:28552882-28553107 | Common:2; Rare:83 | ||||
chr1:28643003-28643237 | Rare:90 | ||||
chr1:28668706-28668830 | Common:1; Rare:47 | ||||
chr1:28736733-28737001 | Common:1; Rare:93 | ||||
chr1:31296747-31297086 | Common:5; Rare:111 | ||||
chr1:32072823-32072952 | Rare:37 | ||||
chr1:32291923-32292156 | Common:1; Rare:82 |