| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:81761461-81761930 | Common:33; Rare:647; Clinvar:7; Clinvar (benign):8 | ||||
| chr3:81761935-81762335 | Common:2; Rare:77 | ||||
| chr3:87227010-87227390 | Common:3; Rare:462; Clinvar:6; Clinvar (benign):7 | ||||
| chr3:88058270-88058903 | Common:9; Rare:495 | ||||
| chr3:88058909-88059377 | Common:18; Rare:1029 | ||||
| chr3:88148973-88149373 | Common:1; Rare:114 | ||||
| chr3:88149450-88150261 | Common:17; Rare:721 | ||||
| chr3:88150335-88151014 | Common:1; Rare:132 | ||||
| chr3:93973240-93973760 | Common:1; Rare:193; Clinvar (benign):2 | ||||
| chr3:93973780-93974350 | Common:4; Rare:421; Clinvar:21 | ||||
| chr3:93979830-93980254 | Common:16; Rare:509; Clinvar:4; Clinvar (benign):8 | ||||
| chr3:93980380-93980500 | Rare:91; Clinvar:4 | ||||
| chr3:94062480-94063934 | Common:13; Rare:814 | ||||
| chr3:97764322-97764796 | Common:4; Rare:469; Clinvar (benign):4 | ||||
| chr3:97821765-97822280 | Common:4; Rare:391 |