| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120094420-120094762 | Common:4; Rare:106 | ||||
| chr3:120742489-120742789 | Common:2; Rare:88 | ||||
| chr3:121749622-121749994 | Common:1; Rare:84 | ||||
| chr3:121834983-121835237 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122384036-122384281 | Common:3; Rare:86 | ||||
| chr3:122416039-122416225 | Common:1; Rare:61 | ||||
| chr3:122564227-122564437 | Common:3; Rare:61 | ||||
| chr3:122795032-122795128 | Common:2; Rare:50 | ||||
| chr3:123067011-123067168 | Rare:39 | ||||
| chr3:123584992-123585305 | Common:1; Rare:103 | ||||
| chr3:123799833-123799931 | Rare:23 | ||||
| chr3:123883969-123884365 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:123949591-123949959 | Common:1; Rare:62 | ||||
| chr3:125520162-125520268 | Rare:34 | ||||
| chr3:126083984-126084219 | Common:2; Rare:79 |