| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39051924-39052046 | Common:1; Rare:43 | ||||
| chr3:39107576-39107684 | Common:2; Rare:34 | ||||
| chr3:39383281-39383452 | Common:2; Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383547-39383726 | Rare:44; Clinvar:2 | ||||
| chr3:39406555-39406764 | Common:6; Rare:88 | ||||
| chr3:40309443-40309803 | Common:9; Rare:123 | ||||
| chr3:40457201-40457388 | Common:3; Rare:91 | ||||
| chr3:40457590-40457990 | Common:4; Rare:118 | ||||
| chr3:41199803-41200143 | Common:2; Rare:96 | ||||
| chr3:41962040-41962378 | Common:4; Rare:81 | ||||
| chr3:42160063-42160263 | Common:2; Rare:39 | ||||
| chr3:42581900-42582138 | Common:3; Rare:73 | ||||
| chr3:42590651-42590958 | Common:3; Rare:94 | ||||
| chr3:42600328-42600749 | Common:3; Rare:168 | ||||
| chr3:42600905-42601000 | Rare:38 |