| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50783577-50783835 | Common:2; Rare:90 | ||||
| chr3:196719-196929 | Common:1; Rare:64 | ||||
| chr3:197011-197334 | Common:3; Rare:111 | ||||
| chr3:197358-197515 | Common:2; Rare:45 | ||||
| chr3:2098627-2098970 | Common:4; Rare:137 | ||||
| chr3:3128844-3129060 | Common:1; Rare:56; Clinvar (benign):1 | ||||
| chr3:4303222-4303412 | Common:2; Rare:74 | ||||
| chr3:4493165-4493359 | Rare:73; Clinvar:1 | ||||
| chr3:8501620-8501960 | Common:2; Rare:126 | ||||
| chr3:9249610-9249742 | Common:1; Rare:34 | ||||
| chr3:9362942-9363099 | Common:2; Rare:58 | ||||
| chr3:9397428-9397697 | Common:1; Rare:102 | ||||
| chr3:9749818-9749991 | Rare:53 | ||||
| chr3:9792414-9792584 | Rare:44 | ||||
| chr3:9792756-9793123 | Common:3; Rare:130 |