| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39107574-39107684 | Common:2; Rare:34 | ||||
| chr3:39383313-39383437 | Common:2; Rare:23; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383582-39383660 | Rare:17; Clinvar:1 | ||||
| chr3:40309496-40309815 | Common:9; Rare:111 | ||||
| chr3:42581913-42582184 | Common:3; Rare:82 | ||||
| chr3:42600377-42600725 | Common:2; Rare:136 | ||||
| chr3:42773211-42773348 | Common:1; Rare:38 | ||||
| chr3:42804272-42804663 | Common:2; Rare:107 | ||||
| chr3:43690823-43690954 | Common:1; Rare:58; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44477646-44477687 | Rare:10 | ||||
| chr3:44624941-44625063 | Common:2; Rare:33 | ||||
| chr3:44729552-44729648 | Common:1; Rare:32 | ||||
| chr3:44761594-44761783 | Common:3; Rare:68 | ||||
| chr3:44861818-44861926 | Common:2; Rare:53 | ||||
| chr3:44976113-44976272 | Common:2; Rare:65 |