| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122416031-122416242 | Common:2; Rare:133 | ||||
| chr3:122496422-122497053 | Common:2; Rare:225 | ||||
| chr3:122514775-122515029 | Common:5; Rare:126 | ||||
| chr3:122564236-122564421 | Common:3; Rare:53 | ||||
| chr3:122680727-122680890 | Rare:99 | ||||
| chr3:122793679-122793958 | Common:6; Rare:122 | ||||
| chr3:122794964-122795178 | Common:6; Rare:176 | ||||
| chr3:123066893-123067180 | Rare:138 | ||||
| chr3:123201730-123201971 | Common:2; Rare:137 | ||||
| chr3:123584977-123585319 | Common:2; Rare:209 | ||||
| chr3:123585483-123585674 | Rare:59 | ||||
| chr3:123799807-123800137 | Common:5; Rare:140 | ||||
| chr3:123961179-123961309 | Rare:57 | ||||
| chr3:124584576-124584759 | Rare:70 | ||||
| chr3:124730317-124730564 | Common:7; Rare:201; Clinvar:6; Clinvar (benign):7 |