Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:9438658-9439100 | Common:2; Rare:75 | ||||
chr1:9687348-9687668 | Common:1; Rare:77 | ||||
chr1:10295492-10295773 | Rare:65; Clinvar:1; Clinvar (benign):4 | ||||
chr1:11109331-11109615 | Rare:50 | ||||
chr1:13993035-13993218 | Common:3; Rare:27 | ||||
chr1:14067178-14067392 | Rare:40 | ||||
chr1:15681451-15681541 | Rare:13 | ||||
chr1:15682397-15682688 | Common:23; Rare:69 | ||||
chr1:15834819-15835169 | Common:2; Rare:154 | ||||
chr1:15835804-15836126 | Common:6; Rare:154 | ||||
chr1:15965327-15965555 | Rare:31 | ||||
chr1:16499238-16499383 | Rare:69 | ||||
chr1:16514468-16514654 | Common:1; Rare:58 | ||||
chr1:16644646-16644805 | Common:1; Rare:3 | ||||
chr1:16889649-16889687 | Rare:13 |