| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:193592890-193593399 | Rare:373; Clinvar:5; Clinvar (benign):6 | ||||
| chr3:194135839-194136581 | Common:5; Rare:378 | ||||
| chr3:194486131-194486538 | Common:13; Rare:154 | ||||
| chr3:194486550-194487199 | Common:18; Rare:613 | ||||
| chr3:194632670-194632945 | Common:2; Rare:71 | ||||
| chr3:194633300-194634020 | Common:17; Rare:416 | ||||
| chr3:194672087-194672676 | Common:11; Rare:410 | ||||
| chr3:195259451-195259637 | Common:1; Rare:37 | ||||
| chr3:195260040-195260377 | Common:7; Rare:187 | ||||
| chr3:195270996-195271397 | Common:6; Rare:359 | ||||
| chr3:195442236-195442479 | Common:1; Rare:85 | ||||
| chr3:195442839-195443471 | Common:15; Rare:514 | ||||
| chr3:195542580-195543090 | Common:4; Rare:157 | ||||
| chr3:195543172-195543543 | Common:12; Rare:322 | ||||
| chr3:195583924-195584057 | Rare:45 |