| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:131381479-131381811 | Common:2; Rare:84 | ||||
| chr3:131502765-131503004 | Common:1; Rare:100 | ||||
| chr3:132627099-132627240 | Common:1; Rare:28 | ||||
| chr3:133661778-133662004 | Rare:52 | ||||
| chr3:134374429-134374691 | Common:1; Rare:81 | ||||
| chr3:134485961-134486065 | Common:2; Rare:40 | ||||
| chr3:135965534-135965844 | Common:1; Rare:123 | ||||
| chr3:136196556-136196688 | Rare:41 | ||||
| chr3:136250182-136250377 | Common:4; Rare:67; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:136752341-136752613 | Common:1; Rare:77 | ||||
| chr3:136818929-136819162 | Common:4; Rare:110 | ||||
| chr3:136862000-136862277 | Common:1; Rare:86 | ||||
| chr3:138115570-138115842 | Common:4; Rare:59 | ||||
| chr3:138174832-138174951 | Common:2; Rare:29 | ||||
| chr3:138594198-138594442 | Rare:70 |