| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39107555-39107695 | Common:3; Rare:42 | ||||
| chr3:39279978-39280141 | Common:2; Rare:24 | ||||
| chr3:39383258-39383443 | Common:2; Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:40309462-40309808 | Common:9; Rare:116 | ||||
| chr3:40457207-40457416 | Common:4; Rare:104 | ||||
| chr3:40524815-40525004 | Common:1; Rare:54 | ||||
| chr3:41962040-41962224 | Common:2; Rare:43 | ||||
| chr3:42149180-42149385 | Rare:51 | ||||
| chr3:42581901-42582150 | Common:3; Rare:75 | ||||
| chr3:42600328-42600778 | Common:3; Rare:174 | ||||
| chr3:42600810-42601000 | Rare:66 | ||||
| chr3:42633289-42633636 | Common:1; Rare:69 | ||||
| chr3:42773206-42773348 | Common:1; Rare:42 | ||||
| chr3:42804252-42804624 | Common:2; Rare:96 | ||||
| chr3:43286449-43286673 | Common:2; Rare:95 |