| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:190073471-190073544 | Common:1; Rare:15 | ||||
| chr3:190120253-190120305 | Rare:24 | ||||
| chr3:194489961-194490072 | Common:1; Rare:25 | ||||
| chr3:194583866-194584027 | Common:11; Rare:56 | ||||
| chr3:194685834-194685897 | Common:1; Rare:20 | ||||
| chr3:194687883-194687907 | Rare:7 | ||||
| chr3:194687913-194688162 | Common:3; Rare:71 | ||||
| chr3:194852370-194852615 | Common:3; Rare:76 | ||||
| chr3:195657926-195658137 | Common:11; Rare:37 | ||||
| chr3:195908019-195908043 | Rare:7 | ||||
| chr3:195990216-195990414 | Rare:23 | ||||
| chr3:196207193-196207305 | Common:1; Rare:25 | ||||
| chr3:196219700-196220006 | Common:1; Rare:52 | ||||
| chr3:196241948-196242264 | Rare:61; Clinvar (pathogenic):1 | ||||
| chr3:196502872-196502928 | Rare:22 |