| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:6680202-6680408 | Common:5; Rare:45 | ||||
| chr3:6717422-6717594 | Common:4; Rare:41 | ||||
| chr3:7204674-7205090 | Common:4; Rare:80 | ||||
| chr3:8767846-8768049 | Common:1; Rare:56 | ||||
| chr3:8954923-8955061 | Common:1; Rare:28 | ||||
| chr3:9180266-9180382 | Common:1; Rare:24 | ||||
| chr3:9396205-9396465 | Common:1; Rare:105 | ||||
| chr3:9396600-9396892 | Common:1; Rare:120 | ||||
| chr3:9398724-9398913 | Rare:57 | ||||
| chr3:9650152-9650367 | Rare:73 | ||||
| chr3:9897977-9898112 | Rare:21 | ||||
| chr3:9915038-9915243 | Common:2; Rare:40 | ||||
| chr3:9915857-9915952 | Rare:17 | ||||
| chr3:9932768-9933082 | Common:1; Rare:115; Clinvar (benign):1 | ||||
| chr3:9946467-9946746 | Common:2; Rare:94 |