| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:101576969-101576991 | Common:1; Rare:1 | ||||
| chr3:101676290-101676517 | Rare:76 | ||||
| chr3:107240630-107240729 | Rare:42 | ||||
| chr3:130111485-130111696 | Common:3; Rare:55 | ||||
| chr3:150408860-150409014 | Rare:45 | ||||
| chr3:157174938-157175223 | Common:3; Rare:125 | ||||
| chr3:169765051-169765222 | Rare:72; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr3:181699453-181699778 | Common:1; Rare:53 | ||||
| chr3:183447477-183447682 | Common:1; Rare:53 | ||||
| chr3:184015636-184015832 | Rare:24 | ||||
| chr3:192514743-192515026 | Common:1; Rare:62 | ||||
| chr3:195657926-195658099 | Common:9; Rare:30 | ||||
| chr3:195990223-195990427 | Rare:25 | ||||
| chr3:197627826-197628019 | Common:6; Rare:74 | ||||
| chr3:197850988-197851262 | Rare:52 |