Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:178731691-178732349 | Common:1; Rare:176; Clinvar:18; Clinvar (benign):13 | ||||
chr2:178769677-178770321 | Common:3; Rare:148; Clinvar:16; Clinvar (benign):13 | ||||
chr2:178773460-178774111 | Common:2; Rare:182; Clinvar:23; Clinvar (benign):16; Clinvar (pathogenic):1 | ||||
chr2:178777418-178777979 | Common:6; Rare:150; Clinvar:27; Clinvar (benign):15 | ||||
chr2:202376105-202376195 | Rare:42 | ||||
chr2:217826630-217826838 | Common:2; Rare:42 | ||||
chr2:217832195-217832450 | Common:1; Rare:52 | ||||
chr2:217837097-217837449 | Rare:74 | ||||
chr2:219426670-219426800 | Common:1; Rare:25; Clinvar (benign):1 | ||||
chr2:226796832-226796996 | Rare:48; Clinvar (pathogenic):1 | ||||
chr2:231057676-231057961 | Rare:59 | ||||
chr2:238142010-238142217 | Common:3; Rare:34 | ||||
chr2:239240539-239240812 | Common:2; Rare:56 | ||||
chr2:239328827-239328964 | Rare:28 | ||||
chr2:240997451-240997677 | Rare:45 |