Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:23940370-23940514 | Common:3; Rare:52 | ||||
chr2:24076284-24076545 | Rare:67 | ||||
chr2:26244602-26244943 | Common:2; Rare:123; Clinvar:5; Clinvar (benign):6 | ||||
chr2:27032862-27032995 | Rare:50 | ||||
chr2:27051526-27051689 | Rare:49 | ||||
chr2:27211920-27212088 | Common:3; Rare:64 | ||||
chr2:27212252-27212379 | Common:1; Rare:64 | ||||
chr2:27323043-27323136 | Rare:22; Clinvar (benign):1 | ||||
chr2:27370319-27370641 | Common:1; Rare:128 | ||||
chr2:27583013-27583095 | Rare:30 | ||||
chr2:27628993-27629055 | Common:1; Rare:29 | ||||
chr2:27663592-27663911 | Rare:113 | ||||
chr2:27771607-27771766 | Common:1; Rare:59 | ||||
chr2:27890429-27890788 | Rare:89 | ||||
chr2:28751716-28751876 | Common:2; Rare:86 |