| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157089010-157089410 | Rare:126 | ||||
| chr3:157120178-157120285 | Rare:23 | ||||
| chr3:157120240-157120928 | Rare:262 | ||||
| chr3:157128449-157128849 | Common:2; Rare:100 | ||||
| chr3:157130457-157130670 | Common:2; Rare:76 | ||||
| chr3:157174851-157175256 | Common:6; Rare:349 | ||||
| chr3:165572770-165572956 | Common:2; Rare:64 | ||||
| chr3:165874654-165875164 | Common:6; Rare:116 | ||||
| chr3:169764805-169765274 | Common:2; Rare:276; Clinvar:28; Clinvar (benign):1; Clinvar (pathogenic):11 | ||||
| chr3:170078695-170079270 | Rare:233 | ||||
| chr3:170425740-170426170 | Common:4; Rare:88 | ||||
| chr3:170997926-170998638 | Common:2; Rare:216; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr3:171002560-171002840 | Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:171045306-171045690 | Common:5; Rare:104 | ||||
| chr3:171838180-171838940 | Common:1; Rare:163 |