| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:167864547-167864856 | Rare:60 | ||||
| chr3:169659684-169660031 | Common:2; Rare:79 | ||||
| chr3:169765058-169765267 | Rare:76; Clinvar (pathogenic):1 | ||||
| chr3:183447501-183447680 | Common:1; Rare:46 | ||||
| chr3:184015650-184015813 | Rare:22 | ||||
| chr3:184582721-184582817 | Common:1; Rare:20 | ||||
| chr3:185418822-185418835 | |||||
| chr3:186664276-186664453 | Common:2; Rare:24 | ||||
| chr3:194583881-194584020 | Common:10; Rare:51 | ||||
| chr3:195657811-195658144 | Common:13; Rare:51 | ||||
| chr3:195990216-195990417 | Rare:24 | ||||
| chr3:196632616-196632804 | Rare:44 | ||||
| chr3:197627826-197628032 | Common:6; Rare:79 | ||||
| chr3:197850988-197851126 | Rare:25 | ||||
| chr4:212548-212644 | Common:1; Rare:29 |