| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:126354080-126354322 | Common:2; Rare:31 | ||||
| chr3:127598197-127598467 | Common:3; Rare:81 | ||||
| chr3:127823135-127823384 | Common:3; Rare:54 | ||||
| chr3:128052161-128052539 | Common:2; Rare:129 | ||||
| chr3:128153319-128153510 | Common:2; Rare:54 | ||||
| chr3:128879392-128879694 | Common:4; Rare:146; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129160971-129161128 | Rare:58 | ||||
| chr3:129161303-129161435 | Common:1; Rare:40 | ||||
| chr3:129183762-129184119 | Common:2; Rare:132 | ||||
| chr3:129249545-129249693 | Common:1; Rare:45 | ||||
| chr3:129278777-129278897 | Common:3; Rare:33 | ||||
| chr3:129439838-129440391 | Common:1; Rare:167; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129893539-129893887 | Rare:135 | ||||
| chr3:130746753-130746853 | Rare:34 | ||||
| chr3:130893905-130894231 | Common:3; Rare:96 |