Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:121530554-121530884 | Common:8; Rare:135 | ||||
chr2:121649424-121649666 | Common:2; Rare:70 | ||||
chr2:121736851-121737104 | Common:4; Rare:88 | ||||
chr2:127294117-127294243 | Common:2; Rare:45; Clinvar (benign):2 | ||||
chr2:127387956-127388244 | Common:7; Rare:125 | ||||
chr2:127811153-127811262 | Rare:33 | ||||
chr2:127858084-127858224 | Common:2; Rare:78 | ||||
chr2:130181529-130181699 | Common:2; Rare:63 | ||||
chr2:130182087-130182279 | Common:1; Rare:69 | ||||
chr2:130342121-130342279 | Rare:65; Clinvar:1 | ||||
chr2:130342642-130342935 | Common:5; Rare:92 | ||||
chr2:130355913-130356065 | Common:1; Rare:41 | ||||
chr2:130372591-130372738 | Rare:49 | ||||
chr2:131492091-131492225 | Common:2; Rare:43 | ||||
chr2:131492724-131492934 | Common:4; Rare:69 |