Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44674046-44674405 | Common:1; Rare:116 | ||||
chr1:44674413-44674792 | Common:3; Rare:101 | ||||
chr1:44739595-44739939 | Common:3; Rare:136 | ||||
chr1:44740115-44740248 | Rare:26 | ||||
chr1:44740332-44740364 | Rare:7 | ||||
chr1:44775012-44775123 | Rare:18 | ||||
chr1:44775276-44775701 | Common:2; Rare:148 | ||||
chr1:44775758-44775874 | Common:1; Rare:43 | ||||
chr1:44799760-44799996 | Common:3; Rare:48 | ||||
chr1:44800087-44800479 | Common:2; Rare:94 | ||||
chr1:44800554-44800667 | Rare:24 | ||||
chr1:44813602-44813965 | Rare:103 | ||||
chr1:44843227-44843313 | Rare:29 | ||||
chr1:44986484-44986909 | Common:3; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
chr1:44987108-44987161 | Common:1; Rare:10 |