| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:167734835-167735302 | Common:5; Rare:151; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735623-167735827 | Rare:55; Clinvar:2 | ||||
| chr3:168095369-168095423 | Rare:12 | ||||
| chr3:169772722-169772808 | Rare:21 | ||||
| chr3:169773331-169773425 | Rare:30 | ||||
| chr3:169812497-169812613 | Common:2; Rare:39 | ||||
| chr3:169966619-169967070 | Common:6; Rare:146 | ||||
| chr3:170870170-170870313 | Rare:70 | ||||
| chr3:170908569-170908824 | Common:1; Rare:71 | ||||
| chr3:171460089-171460526 | Common:2; Rare:99 | ||||
| chr3:172750586-172750797 | Common:3; Rare:59 | ||||
| chr3:173395601-173395930 | Common:2; Rare:121 | ||||
| chr3:173396169-173396527 | Common:2; Rare:74 | ||||
| chr3:173397446-173397820 | Common:4; Rare:119 | ||||
| chr3:173584746-173585009 | Common:1; Rare:57 |