| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9933544-9933863 | Common:2; Rare:128; Clinvar:2 | ||||
| chr3:10026329-10026484 | Rare:45 | ||||
| chr3:10115520-10115708 | Common:3; Rare:68 | ||||
| chr3:10141672-10141870 | Common:1; Rare:91; Clinvar:15; Clinvar (benign):18 | ||||
| chr3:11272227-11272427 | Common:1; Rare:44 | ||||
| chr3:11610083-11610350 | Common:2; Rare:60 | ||||
| chr3:11846849-11847039 | Common:1; Rare:52 | ||||
| chr3:12484333-12484554 | Common:5; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12556905-12557144 | Common:5; Rare:84 | ||||
| chr3:12664059-12664355 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:13479983-13480335 | Common:3; Rare:90 | ||||
| chr3:14124703-14125167 | Common:4; Rare:138; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178573-14178881 | Common:2; Rare:159; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:14402405-14402632 | Common:1; Rare:61 | ||||
| chr3:14651463-14651833 | Rare:115 |