Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:134918580-134918894 | Common:1; Rare:130 | ||||
chr2:135052132-135052310 | Common:2; Rare:57; Clinvar (benign):1 | ||||
chr2:135530689-135530988 | Common:4; Rare:71 | ||||
chr2:135531153-135531606 | Common:1; Rare:101 | ||||
chr2:135741617-135742014 | Common:3; Rare:139 | ||||
chr2:135876261-135876610 | Common:1; Rare:104 | ||||
chr2:135985065-135985177 | Common:1; Rare:32 | ||||
chr2:135985387-135985699 | Common:4; Rare:130; Clinvar (benign):1 | ||||
chr2:138501639-138502002 | Common:4; Rare:135 | ||||
chr2:138780338-138780498 | Rare:45 | ||||
chr2:144332433-144332764 | Common:1; Rare:129 | ||||
chr2:147844231-147844831 | Common:7; Rare:195 | ||||
chr2:148020642-148021444 | Common:2; Rare:184; Clinvar (benign):2 | ||||
chr2:148021571-148021683 | Rare:24; Clinvar (benign):1 | ||||
chr2:148644509-148644793 | Rare:86 |