| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121834987-121835234 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383192-122383313 | Common:1; Rare:39 | ||||
| chr3:122384151-122384227 | Rare:30 | ||||
| chr3:122416039-122416225 | Common:1; Rare:61 | ||||
| chr3:122564252-122564521 | Common:3; Rare:79 | ||||
| chr3:123066949-123067172 | Rare:56 | ||||
| chr3:123585035-123585284 | Common:1; Rare:77 | ||||
| chr3:123585491-123585553 | Rare:10 | ||||
| chr3:123692308-123692468 | Rare:38 | ||||
| chr3:125375231-125375391 | Rare:43 | ||||
| chr3:127598219-127598458 | Common:3; Rare:71 | ||||
| chr3:127822451-127822622 | Rare:40 | ||||
| chr3:128052170-128052532 | Common:2; Rare:122 | ||||
| chr3:128123753-128124037 | Rare:77 | ||||
| chr3:128153383-128153496 | Rare:34 |