| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33097104-33097279 | Common:2; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33798527-33798662 | Common:2; Rare:50 | ||||
| chr3:39051917-39052019 | Common:1; Rare:34 | ||||
| chr3:40309486-40309807 | Common:9; Rare:110 | ||||
| chr3:40457207-40457368 | Common:2; Rare:78 | ||||
| chr3:42581948-42582083 | Common:2; Rare:39 | ||||
| chr3:42600418-42600709 | Common:2; Rare:109 | ||||
| chr3:44761594-44761820 | Common:3; Rare:80 | ||||
| chr3:44976126-44976272 | Common:2; Rare:63 | ||||
| chr3:45146301-45146525 | Common:1; Rare:79 | ||||
| chr3:45995811-45995868 | Rare:14; Clinvar:1 | ||||
| chr3:47380803-47381051 | Rare:76 | ||||
| chr3:47475816-47476058 | Common:3; Rare:103 | ||||
| chr3:47513322-47513510 | Common:1; Rare:50 | ||||
| chr3:48440056-48440303 | Common:1; Rare:92 |