| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121835046-121835231 | Common:2; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:122383192-122383310 | Common:1; Rare:38 | ||||
| chr3:122384054-122384281 | Common:3; Rare:81 | ||||
| chr3:122416075-122416200 | Rare:33 | ||||
| chr3:122514878-122515006 | Common:1; Rare:35 | ||||
| chr3:122564243-122564419 | Common:3; Rare:51 | ||||
| chr3:123585028-123585284 | Common:1; Rare:81 | ||||
| chr3:125375180-125375419 | Rare:68 | ||||
| chr3:127591077-127591249 | Common:1; Rare:40 | ||||
| chr3:127598224-127598446 | Common:3; Rare:58 | ||||
| chr3:128879440-128879675 | Common:4; Rare:118; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129161013-129161123 | Rare:42 | ||||
| chr3:129183814-129184026 | Common:2; Rare:67 | ||||
| chr3:129249492-129249678 | Common:3; Rare:57 | ||||
| chr3:129439876-129440254 | Common:1; Rare:111; Clinvar:1; Clinvar (benign):1 |