| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:96814117-96814162 | Rare:11 | ||||
| chr3:96814375-96814677 | Rare:112 | ||||
| chr3:97764448-97764833 | Common:1; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821939-97822097 | Rare:55 | ||||
| chr3:98732429-98732508 | Rare:15 | ||||
| chr3:98732647-98732746 | Rare:20 | ||||
| chr3:98901664-98902014 | Common:1; Rare:133 | ||||
| chr3:99817562-99817920 | Rare:103 | ||||
| chr3:99876140-99876414 | Common:3; Rare:76 | ||||
| chr3:100260688-100261021 | Rare:89 | ||||
| chr3:100334666-100334780 | Common:1; Rare:54 | ||||
| chr3:100401068-100401215 | Rare:43 | ||||
| chr3:100401421-100401592 | Common:1; Rare:31 | ||||
| chr3:100492413-100492606 | Common:2; Rare:64 | ||||
| chr3:100709263-100709714 | Common:6; Rare:137; Clinvar (benign):1 |