| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:154276853-154277077 | Rare:54 | ||||
| chr3:154300661-154300725 | Rare:19 | ||||
| chr3:155664966-155665098 | Rare:20 | ||||
| chr3:156524329-156524535 | Common:1; Rare:40 | ||||
| chr3:156536163-156536430 | Common:2; Rare:49 | ||||
| chr3:156816982-156817330 | Rare:103 | ||||
| chr3:157174857-157175322 | Common:3; Rare:195 | ||||
| chr3:158653157-158653463 | Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:159732263-159732392 | Common:1; Rare:23 | ||||
| chr3:159763138-159763167 | Rare:5 | ||||
| chr3:159765880-159765986 | Rare:20 | ||||
| chr3:159796594-159796655 | Rare:8 | ||||
| chr3:167811067-167811259 | Rare:28 | ||||
| chr3:167864707-167864860 | Rare:29 | ||||
| chr3:169132813-169132832 | Rare:2 |