Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:178688718-178689074 | Common:2; Rare:95; Clinvar:4; Clinvar (benign):3 | ||||
chr2:188996131-188996416 | Common:12; Rare:62; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr2:197495297-197495606 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
chr2:197498835-197499071 | Common:3; Rare:68; Clinvar (benign):1 | ||||
chr2:202376111-202376205 | Rare:52 | ||||
chr2:210023108-210023347 | Common:2; Rare:63 | ||||
chr2:210050333-210050568 | Rare:39 | ||||
chr2:215386888-215387206 | Common:2; Rare:71 | ||||
chr2:217812126-217812438 | Common:3; Rare:59 | ||||
chr2:217906858-217906965 | Common:3; Rare:16 | ||||
chr2:217910132-217910385 | Common:2; Rare:38 | ||||
chr2:218277037-218277247 | Common:1; Rare:48 | ||||
chr2:235577596-235577880 | Common:2; Rare:61 | ||||
chr2:237359033-237359223 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr2:237408524-237408691 | Rare:22 |