| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120094326-120094749 | Common:4; Rare:136 | ||||
| chr3:120596221-120596497 | Rare:112 | ||||
| chr3:120682095-120682480 | Common:1; Rare:77; Clinvar:7; Clinvar (pathogenic):1 | ||||
| chr3:120742503-120742794 | Common:2; Rare:83 | ||||
| chr3:121749131-121749293 | Rare:27 | ||||
| chr3:121749637-121750021 | Common:1; Rare:88 | ||||
| chr3:121834987-121835241 | Common:3; Rare:85; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383190-122383332 | Common:1; Rare:44 | ||||
| chr3:122384036-122384296 | Common:4; Rare:91 | ||||
| chr3:122416039-122416225 | Common:1; Rare:61 | ||||
| chr3:122514853-122515023 | Common:1; Rare:50 | ||||
| chr3:122564195-122564552 | Common:4; Rare:96 | ||||
| chr3:123066949-123067172 | Rare:56 | ||||
| chr3:123124138-123124332 | Common:2; Rare:57 | ||||
| chr3:123201710-123201977 | Common:1; Rare:80 |