| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119676909-119677163 | Common:17; Rare:80 | ||||
| chr3:120742507-120742789 | Common:2; Rare:79 | ||||
| chr3:121834987-121835238 | Common:3; Rare:82; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122384108-122384292 | Common:3; Rare:68 | ||||
| chr3:122564112-122564427 | Common:4; Rare:93 | ||||
| chr3:123585032-123585305 | Common:1; Rare:83 | ||||
| chr3:123692357-123692437 | Rare:17 | ||||
| chr3:124730317-124730595 | Common:4; Rare:129; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:125520035-125520298 | Rare:95 | ||||
| chr3:125595441-125595751 | Common:2; Rare:92 | ||||
| chr3:126083901-126084189 | Common:4; Rare:69 | ||||
| chr3:126957035-126957547 | Common:5; Rare:114 | ||||
| chr3:127598223-127598461 | Common:3; Rare:69 | ||||
| chr3:128052170-128052515 | Common:2; Rare:117 | ||||
| chr3:128153383-128153487 | Rare:30 |