| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:45995743-45995911 | Rare:62; Clinvar:2 | ||||
| chr3:46976630-46977150 | Common:8; Rare:222 | ||||
| chr3:46979508-46979857 | Common:5; Rare:174; Clinvar:3 | ||||
| chr3:47162980-47163360 | Common:1; Rare:122 | ||||
| chr3:47163918-47164473 | Common:3; Rare:273 | ||||
| chr3:47380774-47381083 | Rare:198 | ||||
| chr3:47475775-47476107 | Common:8; Rare:238 | ||||
| chr3:47513285-47513589 | Common:2; Rare:182 | ||||
| chr3:47513635-47513802 | Common:2; Rare:96 | ||||
| chr3:47781758-47782054 | Rare:204 | ||||
| chr3:47802859-47802974 | Rare:36 | ||||
| chr3:47803034-47803197 | Common:1; Rare:85 | ||||
| chr3:47824552-47825132 | Common:2; Rare:224 | ||||
| chr3:48088780-48089102 | Rare:198 | ||||
| chr3:48089181-48089298 | Rare:39 |