| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32491708-32492130 | Common:4; Rare:81 | ||||
| chr3:33407708-33407735 | Rare:2 | ||||
| chr3:33409449-33409747 | Rare:48 | ||||
| chr3:33841670-33842057 | Common:1; Rare:90 | ||||
| chr3:37055128-37055266 | Rare:36 | ||||
| chr3:37784793-37785072 | Common:1; Rare:65 | ||||
| chr3:38001553-38001848 | Rare:95 | ||||
| chr3:38011437-38011558 | Rare:38; Clinvar (pathogenic):1 | ||||
| chr3:38455443-38455470 | Rare:4 | ||||
| chr3:39411652-39412006 | Common:1; Rare:88; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:40238324-40238541 | Common:2; Rare:46 | ||||
| chr3:40453163-40453435 | Common:6; Rare:61 | ||||
| chr3:41200952-41201255 | Common:2; Rare:59 | ||||
| chr3:41207609-41207772 | Rare:31 | ||||
| chr3:41225226-41225859 | Rare:137; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 |