| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169764838-169765341 | Common:3; Rare:418; Clinvar:45; Clinvar (pathogenic):18 | ||||
| chr3:169871520-169871870 | Rare:46 | ||||
| chr3:170046586-170046922 | Common:2; Rare:65 | ||||
| chr3:170180709-170181214 | Common:1; Rare:140 | ||||
| chr3:170320794-170320901 | Common:1; Rare:19 | ||||
| chr3:170356600-170357058 | Common:9; Rare:402 | ||||
| chr3:170506563-170506795 | Rare:33 | ||||
| chr3:170751605-170752005 | Common:3; Rare:105 | ||||
| chr3:171404096-171405042 | Common:18; Rare:292 | ||||
| chr3:171461040-171461650 | Common:7; Rare:115 | ||||
| chr3:171967230-171967600 | Common:2; Rare:62 | ||||
| chr3:172203920-172204210 | Rare:38 | ||||
| chr3:172516744-172517144 | Common:5; Rare:143 | ||||
| chr3:172536591-172536830 | Rare:84 | ||||
| chr3:172623692-172624130 | Common:4; Rare:159 |