| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:170359475-170359549 | Rare:18 | ||||
| chr3:177196465-177196783 | Common:2; Rare:107 | ||||
| chr3:179147916-179148202 | Common:4; Rare:85 | ||||
| chr3:179323757-179323858 | Common:2; Rare:31 | ||||
| chr3:179604628-179604841 | Common:1; Rare:73 | ||||
| chr3:180601981-180602264 | Common:1; Rare:96 | ||||
| chr3:180989671-180989782 | Rare:45; Clinvar:1 | ||||
| chr3:182793371-182793586 | Common:3; Rare:52 | ||||
| chr3:183099494-183099742 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:183555639-183555814 | Common:1; Rare:43 | ||||
| chr3:183884848-183885036 | Rare:64 | ||||
| chr3:184135248-184135387 | Common:2; Rare:37; Clinvar:2 | ||||
| chr3:184174620-184174924 | Common:2; Rare:84 | ||||
| chr3:184249557-184249685 | Rare:37 | ||||
| chr3:184314440-184314661 | Common:3; Rare:65 |