| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:156676544-156676638 | Rare:16 | ||||
| chr3:156826154-156826381 | Common:3; Rare:76 | ||||
| chr3:156826613-156826675 | Rare:16 | ||||
| chr3:157159816-157159888 | Rare:19 | ||||
| chr3:157160038-157160315 | Rare:117 | ||||
| chr3:157543233-157543309 | Rare:15 | ||||
| chr3:158107690-158107820 | Common:1; Rare:26 | ||||
| chr3:158110029-158110194 | Rare:40 | ||||
| chr3:158571007-158571391 | Common:3; Rare:112 | ||||
| chr3:158644481-158644702 | Common:5; Rare:78; Clinvar:1; Clinvar (benign):6 | ||||
| chr3:158672569-158672609 | Common:1; Rare:8 | ||||
| chr3:158672626-158672716 | Rare:28 | ||||
| chr3:158732026-158732431 | Common:11; Rare:125 | ||||
| chr3:158801967-158802168 | Common:2; Rare:94 | ||||
| chr3:159763610-159763734 | Rare:37 |