| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:159732269-159732385 | Common:1; Rare:16 | ||||
| chr3:169765011-169765243 | Rare:97; Clinvar:6; Clinvar (pathogenic):3 | ||||
| chr3:171874281-171874553 | Common:3; Rare:47 | ||||
| chr3:183447414-183447674 | Common:2; Rare:67 | ||||
| chr3:194575243-194575394 | Common:2; Rare:34 | ||||
| chr3:194583866-194584027 | Common:11; Rare:56 | ||||
| chr3:195990227-195990421 | Rare:25 | ||||
| chr3:197627833-197628009 | Common:6; Rare:64 | ||||
| chr3:198157310-198157538 | Common:2; Rare:50 | ||||
| chr4:6673862-6673923 | Common:1; Rare:27 | ||||
| chr4:21447778-21447846 | Rare:11 | ||||
| chr4:38667227-38667368 | Rare:22 | ||||
| chr4:39319779-39320068 | Rare:39 | ||||
| chr4:48954830-48954951 | Rare:25 | ||||
| chr4:52712230-52712513 | Common:4; Rare:72 |