| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:164338784-164338977 | Rare:50 | ||||
| chr3:164401527-164401674 | Common:2; Rare:34 | ||||
| chr3:165071906-165072080 | Common:2; Rare:28 | ||||
| chr3:165923766-165923780 | Common:1; Rare:1 | ||||
| chr3:166435263-166435326 | Common:1; Rare:13 | ||||
| chr3:166843550-166843678 | Rare:19 | ||||
| chr3:168249535-168249691 | Common:1; Rare:41 | ||||
| chr3:168249840-168250106 | Common:1; Rare:72 | ||||
| chr3:169764796-169764825 | Rare:5; Clinvar:1 | ||||
| chr3:169764839-169765267 | Common:1; Rare:149; Clinvar:18; Clinvar (pathogenic):6 | ||||
| chr3:170341403-170341525 | Common:1; Rare:19 | ||||
| chr3:171110735-171111159 | Common:3; Rare:78 | ||||
| chr3:171339199-171339499 | Rare:48 | ||||
| chr3:171710401-171710517 | Common:1; Rare:31 | ||||
| chr3:171746619-171746854 | Rare:52 |