| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178593839-178594007 | Common:1; Rare:50; Clinvar:5; Clinvar (benign):4 | ||||
| chr2:178602280-178602843 | Common:1; Rare:97; Clinvar:9; Clinvar (benign):8 | ||||
| chr2:178609822-178610157 | Common:1; Rare:91; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:178685284-178685601 | Common:2; Rare:63; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:178689051-178689370 | Common:1; Rare:96; Clinvar:9; Clinvar (benign):8 | ||||
| chr2:178719415-178719646 | Rare:70; Clinvar:4; Clinvar (benign):7 | ||||
| chr2:188990093-188990370 | Rare:80; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr2:188994036-188994330 | Common:1; Rare:81; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
| chr2:188994532-188994831 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr2:188996175-188996494 | Common:12; Rare:70; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr2:188997166-188997390 | Common:5; Rare:58; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):4 | ||||
| chr2:188999466-188999894 | Common:1; Rare:109; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):16 | ||||
| chr2:189003979-189004364 | Rare:115; Clinvar:10; Clinvar (benign):8; Clinvar (pathogenic):23 | ||||
| chr2:202376111-202376180 | Rare:30 | ||||
| chr2:216677895-216678166 | Rare:63 |