| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160755113-160755179 | Common:2; Rare:19 | ||||
| chr3:161104726-161104859 | Common:2; Rare:28 | ||||
| chr3:161104942-161105013 | Rare:20 | ||||
| chr3:161105015-161105436 | Common:4; Rare:132 | ||||
| chr3:161221209-161221360 | Common:2; Rare:50 | ||||
| chr3:167734811-167735257 | Common:5; Rare:146; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735591-167735768 | Rare:47; Clinvar:1 | ||||
| chr3:168094777-168094960 | Common:1; Rare:36 | ||||
| chr3:168094963-168095055 | Common:1; Rare:16 | ||||
| chr3:169769581-169769634 | Rare:18 | ||||
| chr3:169773325-169773424 | Rare:30 | ||||
| chr3:169966632-169966858 | Common:2; Rare:89 | ||||
| chr3:170870166-170870280 | Rare:63 | ||||
| chr3:170908564-170908842 | Common:1; Rare:77 | ||||
| chr3:171460258-171460609 | Rare:84 |