| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:188947200-188947242 | Rare:7 | ||||
| chr3:189171803-189172122 | Common:2; Rare:49 | ||||
| chr3:189789452-189789842 | Common:5; Rare:62; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:190120315-190120476 | Common:1; Rare:64; Clinvar (pathogenic):1 | ||||
| chr3:190120862-190121004 | Rare:48 | ||||
| chr3:190321971-190322566 | Common:4; Rare:176; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:190322883-190322986 | Rare:13 | ||||
| chr3:190513903-190514149 | Common:2; Rare:66 | ||||
| chr3:191329333-191329633 | Common:3; Rare:86 | ||||
| chr3:192917836-192918023 | Common:2; Rare:84 | ||||
| chr3:193554758-193554990 | Common:1; Rare:59 | ||||
| chr3:193593091-193593382 | Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194136215-194136338 | Common:2; Rare:26 | ||||
| chr3:194487008-194487140 | Common:3; Rare:61 | ||||
| chr3:194672153-194672457 | Common:1; Rare:93 |