| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:133661780-133662033 | Rare:60 | ||||
| chr3:134374395-134374600 | Common:1; Rare:56 | ||||
| chr3:134485381-134485766 | Rare:88 | ||||
| chr3:134485957-134486296 | Common:3; Rare:118 | ||||
| chr3:135965522-135965844 | Common:1; Rare:126 | ||||
| chr3:135965928-135966236 | Common:3; Rare:93 | ||||
| chr3:136196562-136196614 | Rare:15 | ||||
| chr3:136250195-136250396 | Common:4; Rare:81; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr3:136752341-136752701 | Common:1; Rare:117 | ||||
| chr3:136862000-136862298 | Common:1; Rare:97 | ||||
| chr3:138115564-138115720 | Common:4; Rare:39 | ||||
| chr3:138174858-138174965 | Common:1; Rare:24 | ||||
| chr3:138187156-138187578 | Common:1; Rare:123 | ||||
| chr3:138329802-138330090 | Common:1; Rare:63 | ||||
| chr3:138348342-138348747 | Common:2; Rare:109 |