| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160755452-160755673 | Common:1; Rare:82 | ||||
| chr3:160756162-160756476 | Rare:80 | ||||
| chr3:161105265-161105412 | Common:2; Rare:55 | ||||
| chr3:161221213-161221383 | Common:2; Rare:55 | ||||
| chr3:167734794-167735071 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735626-167735747 | Rare:32 | ||||
| chr3:169146513-169146612 | Rare:43 | ||||
| chr3:169147291-169147391 | Common:1; Rare:24 | ||||
| chr3:169773341-169773425 | Rare:26 | ||||
| chr3:170102619-170102840 | Rare:58 | ||||
| chr3:170870170-170870286 | Rare:61 | ||||
| chr3:170908580-170908839 | Common:1; Rare:72 | ||||
| chr3:172711038-172711143 | Rare:51 | ||||
| chr3:172750578-172750784 | Common:3; Rare:59 | ||||
| chr3:173397621-173397810 | Rare:73 |