| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:139539498-139539788 | Common:3; Rare:98 | ||||
| chr3:140941646-140941907 | Common:2; Rare:101 | ||||
| chr3:141368254-141368580 | Rare:71 | ||||
| chr3:141386753-141386930 | Rare:21 | ||||
| chr3:141738109-141738365 | Common:1; Rare:107 | ||||
| chr3:143001351-143001670 | Common:4; Rare:117 | ||||
| chr3:146070848-146071107 | Common:1; Rare:60; Clinvar:1 | ||||
| chr3:146160882-146161098 | Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:146544520-146544779 | Common:3; Rare:62 | ||||
| chr3:149129542-149129701 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377465-149377817 | Common:1; Rare:103 | ||||
| chr3:149657961-149658197 | Rare:51 | ||||
| chr3:149970831-149971020 | Rare:92 | ||||
| chr3:149971096-149971312 | Common:4; Rare:88 | ||||
| chr3:150408131-150408298 | Common:1; Rare:64 |