| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:132660049-132660454 | Common:2; Rare:84 | ||||
| chr3:132660557-132661370 | Common:5; Rare:310 | ||||
| chr3:132674774-132675189 | Common:2; Rare:142 | ||||
| chr3:132722042-132722167 | Rare:39; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:132722176-132723038 | Common:21; Rare:342; Clinvar:16; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr3:133448793-133449195 | Common:8; Rare:140 | ||||
| chr3:133573150-133574719 | Common:25; Rare:1094 | ||||
| chr3:133661310-133661710 | Common:1; Rare:70 | ||||
| chr3:133661753-133662081 | Rare:193 | ||||
| chr3:133805490-133805921 | Common:4; Rare:286 | ||||
| chr3:133806191-133806309 | Rare:28 | ||||
| chr3:133895285-133896120 | Common:9; Rare:377 | ||||
| chr3:134029859-134030646 | Common:9; Rare:222 | ||||
| chr3:134249125-134250460 | Common:13; Rare:369 | ||||
| chr3:134250724-134251146 | Common:4; Rare:307 |