Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:23927067-23927325 | Common:3; Rare:90 | ||||
chr2:23940379-23940514 | Common:3; Rare:49 | ||||
chr2:24047359-24047628 | Common:1; Rare:70 | ||||
chr2:24076205-24076602 | Rare:109 | ||||
chr2:24123272-24123478 | Common:1; Rare:51 | ||||
chr2:26033799-26034159 | Common:3; Rare:123 | ||||
chr2:26244592-26244931 | Common:2; Rare:121; Clinvar:5; Clinvar (benign):7 | ||||
chr2:26345825-26346165 | Common:1; Rare:101 | ||||
chr2:26764188-26764332 | Common:1; Rare:57 | ||||
chr2:27032872-27032995 | Rare:46 | ||||
chr2:27212252-27212364 | Common:1; Rare:57 | ||||
chr2:27323063-27323155 | Rare:21 | ||||
chr2:27356754-27356850 | Rare:25 | ||||
chr2:27370317-27370641 | Common:1; Rare:128 | ||||
chr2:27628876-27629061 | Common:1; Rare:78 |