| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42600893-42601000 | Rare:42 | ||||
| chr3:42804242-42804669 | Common:2; Rare:117 | ||||
| chr3:42843692-42844055 | Common:2; Rare:49 | ||||
| chr3:43286471-43286661 | Common:2; Rare:81 | ||||
| chr3:43690763-43691013 | Common:4; Rare:136; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:43691554-43691606 | Common:1; Rare:11 | ||||
| chr3:44338387-44338518 | Common:1; Rare:48 | ||||
| chr3:44338706-44338830 | Common:3; Rare:43 | ||||
| chr3:44477640-44477746 | Common:1; Rare:21 | ||||
| chr3:44555020-44555241 | Common:1; Rare:51 | ||||
| chr3:44584848-44584981 | Rare:33 | ||||
| chr3:44624845-44625095 | Common:2; Rare:70 | ||||
| chr3:44712578-44712704 | Common:1; Rare:49 | ||||
| chr3:44729525-44729688 | Common:1; Rare:62 | ||||
| chr3:44761507-44761691 | Common:3; Rare:98 |