| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123585501-123585553 | Rare:9 | ||||
| chr3:123700948-123701310 | Rare:75; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:124730324-124730468 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:125375160-125375358 | Rare:55 | ||||
| chr3:125520163-125520288 | Rare:38 | ||||
| chr3:126084103-126084365 | Common:1; Rare:96 | ||||
| chr3:127598217-127598458 | Common:3; Rare:72 | ||||
| chr3:127628970-127629211 | Common:1; Rare:79 | ||||
| chr3:127672720-127673007 | Common:4; Rare:132 | ||||
| chr3:127822459-127822638 | Rare:40 | ||||
| chr3:128052173-128052495 | Common:2; Rare:109 | ||||
| chr3:128879421-128879676 | Common:4; Rare:125; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129161017-129161466 | Common:2; Rare:141 | ||||
| chr3:129183814-129184075 | Common:2; Rare:89 | ||||
| chr3:129249492-129249712 | Common:3; Rare:66 |