| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23916916-23917218 | Rare:114 | ||||
| chr3:24494764-24494906 | Rare:35 | ||||
| chr3:25663731-25664026 | Common:2; Rare:62 | ||||
| chr3:25664886-25664923 | Rare:13 | ||||
| chr3:25783387-25783641 | Common:2; Rare:81; Clinvar (benign):3 | ||||
| chr3:25790021-25790118 | Common:2; Rare:36 | ||||
| chr3:27484375-27484699 | Common:2; Rare:109 | ||||
| chr3:28348612-28348727 | Rare:27 | ||||
| chr3:28348813-28348858 | Rare:13 | ||||
| chr3:31532283-31532617 | Common:3; Rare:102 | ||||
| chr3:32570771-32570881 | Rare:55 | ||||
| chr3:33096732-33096930 | Common:1; Rare:52 | ||||
| chr3:33097110-33097257 | Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:33718071-33718291 | Rare:80 | ||||
| chr3:33798495-33798893 | Common:3; Rare:138 |