| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121749631-121750031 | Common:1; Rare:92 | ||||
| chr3:121834987-121835231 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122022209-122022330 | Common:4; Rare:29 | ||||
| chr3:122383192-122383323 | Common:1; Rare:41 | ||||
| chr3:122384041-122384262 | Rare:80 | ||||
| chr3:122514873-122515026 | Common:1; Rare:41 | ||||
| chr3:122564244-122564421 | Common:3; Rare:52 | ||||
| chr3:123066893-123067125 | Rare:58 | ||||
| chr3:123585035-123585305 | Common:1; Rare:82 | ||||
| chr3:123585511-123585553 | Rare:7 | ||||
| chr3:123961194-123961483 | Common:3; Rare:118 | ||||
| chr3:124730340-124730468 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:125375242-125375425 | Rare:55 | ||||
| chr3:125595262-125595352 | Common:2; Rare:32 | ||||
| chr3:127598223-127598458 | Common:3; Rare:68 |