Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:113889766-113890165 | Common:8; Rare:128 | ||||
chr2:118014056-118014221 | Common:2; Rare:93 | ||||
chr2:119366804-119367059 | Common:1; Rare:74 | ||||
chr2:121285200-121285340 | Rare:47 | ||||
chr2:121530618-121530884 | Common:5; Rare:112 | ||||
chr2:121649452-121649645 | Common:2; Rare:61 | ||||
chr2:127294100-127294196 | Common:2; Rare:38; Clinvar (benign):2 | ||||
chr2:127387958-127388282 | Common:7; Rare:141 | ||||
chr2:127526452-127526607 | Common:1; Rare:46 | ||||
chr2:127811121-127811282 | Common:1; Rare:55 | ||||
chr2:128091038-128091333 | Common:8; Rare:99 | ||||
chr2:130181553-130181696 | Common:1; Rare:48 | ||||
chr2:130182101-130182294 | Common:2; Rare:69 | ||||
chr2:130342127-130342217 | Rare:37 | ||||
chr2:130342678-130342923 | Common:2; Rare:78 |