| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160565260-160565842 | Common:3; Rare:193 | ||||
| chr3:160755448-160755664 | Common:1; Rare:82 | ||||
| chr3:160755922-160756290 | Common:1; Rare:92 | ||||
| chr3:165196349-165196506 | Common:2; Rare:42 | ||||
| chr3:167734818-167735237 | Common:3; Rare:136; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735609-167735746 | Rare:33 | ||||
| chr3:168095862-168096226 | Common:1; Rare:119 | ||||
| chr3:169147313-169147493 | Common:2; Rare:44 | ||||
| chr3:169769543-169769651 | Common:1; Rare:42 | ||||
| chr3:169769801-169769888 | Common:2; Rare:17 | ||||
| chr3:169772765-169772837 | Rare:16 | ||||
| chr3:169773331-169773415 | Rare:25 | ||||
| chr3:169966727-169966858 | Rare:56 | ||||
| chr3:170181411-170181605 | Common:3; Rare:60 | ||||
| chr3:170870163-170870312 | Rare:76 |