| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33277334-33277499 | Common:1; Rare:47 | ||||
| chr3:33798546-33798809 | Common:3; Rare:90 | ||||
| chr3:33798815-33798973 | Rare:62 | ||||
| chr3:33798982-33799115 | Rare:43 | ||||
| chr3:35639211-35639529 | Common:1; Rare:81 | ||||
| chr3:36992692-36992943 | Rare:80 | ||||
| chr3:36993052-36993627 | Common:2; Rare:208; Clinvar:41; Clinvar (benign):20; Clinvar (pathogenic):4 | ||||
| chr3:36993671-36993854 | Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:37175866-37176068 | Rare:49 | ||||
| chr3:37176104-37176410 | Common:1; Rare:84 | ||||
| chr3:37243007-37243328 | Common:5; Rare:88 | ||||
| chr3:37861704-37861984 | Common:1; Rare:57 | ||||
| chr3:38029621-38029864 | Common:1; Rare:49 | ||||
| chr3:38137065-38137447 | Common:1; Rare:87 | ||||
| chr3:38165467-38165860 | Common:1; Rare:137 |