| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:182979423-182980492 | Common:8; Rare:504 | ||||
| chr3:182980449-182980651 | Rare:234 | ||||
| chr3:182980624-182981319 | Common:4; Rare:181 | ||||
| chr3:183098727-183099311 | Common:4; Rare:294 | ||||
| chr3:183099409-183099818 | Common:12; Rare:643; Clinvar:17; Clinvar (benign):28; Clinvar (pathogenic):5 | ||||
| chr3:183162560-183163024 | Common:21; Rare:259 | ||||
| chr3:183252722-183253860 | Common:18; Rare:584 | ||||
| chr3:183253890-183254666 | Common:6; Rare:428 | ||||
| chr3:183254586-183254825 | Rare:56 | ||||
| chr3:183287140-183287500 | Common:30; Rare:183 | ||||
| chr3:183287525-183287925 | Common:1; Rare:135 | ||||
| chr3:183400311-183400711 | Common:2; Rare:127 | ||||
| chr3:183427942-183428440 | Common:4; Rare:222 | ||||
| chr3:183428500-183428930 | Common:10; Rare:405 | ||||
| chr3:183428900-183429160 | Common:3; Rare:51 |