Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43367961-43368190 | Rare:60 | ||||
chr1:43389763-43389945 | Common:3; Rare:78 | ||||
chr1:43946649-43946974 | Rare:88 | ||||
chr1:44674413-44674769 | Common:3; Rare:95 | ||||
chr1:44739647-44739897 | Common:2; Rare:99 | ||||
chr1:44775505-44775609 | Rare:48 | ||||
chr1:44986552-44986730 | Common:2; Rare:32; Clinvar (benign):1 | ||||
chr1:45500056-45500341 | Common:1; Rare:70; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521838-45522074 | Common:1; Rare:95 | ||||
chr1:45687059-45687351 | Common:1; Rare:75 | ||||
chr1:45688059-45688258 | Common:1; Rare:57 | ||||
chr1:45750621-45750815 | Rare:70 | ||||
chr1:46198420-46198488 | Common:1; Rare:25; Clinvar:1 | ||||
chr1:46303341-46303769 | Common:2; Rare:117 | ||||
chr1:47333604-47333959 | Common:3; Rare:113 |