Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:121755379-121755763 | Common:5; Rare:125 | ||||
chr2:127294098-127294205 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
chr2:127811121-127811298 | Common:1; Rare:66 | ||||
chr2:128091123-128091335 | Common:3; Rare:66 | ||||
chr2:130181568-130181780 | Common:3; Rare:93 | ||||
chr2:130342118-130342217 | Rare:43; Clinvar:1 | ||||
chr2:130342645-130342923 | Common:4; Rare:85 | ||||
chr2:131105202-131105356 | Common:1; Rare:66 | ||||
chr2:131492754-131493097 | Common:8; Rare:103 | ||||
chr2:134918690-134918877 | Rare:84 | ||||
chr2:135531195-135531514 | Common:1; Rare:59 | ||||
chr2:135876400-135876650 | Rare:65 | ||||
chr2:135985404-135985496 | Rare:38 | ||||
chr2:135985498-135985696 | Common:4; Rare:86; Clinvar (benign):1 | ||||
chr2:137964366-137964562 | Common:1; Rare:41 |