| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:182985830-182986049 | Common:2; Rare:39 | ||||
| chr3:183099436-183099711 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183253040-183253265 | Common:3; Rare:70 | ||||
| chr3:183311080-183311210 | Rare:24 | ||||
| chr3:183428221-183428521 | Rare:57 | ||||
| chr3:183635516-183635707 | Common:2; Rare:60 | ||||
| chr3:183697718-183697934 | Common:1; Rare:96 | ||||
| chr3:183698036-183698104 | Rare:26 | ||||
| chr3:183884727-183884969 | Rare:100 | ||||
| chr3:184017418-184017546 | Common:1; Rare:26 | ||||
| chr3:184017864-184018103 | Common:1; Rare:75 | ||||
| chr3:184135215-184135398 | Common:2; Rare:55; Clinvar:5 | ||||
| chr3:184155297-184155338 | Rare:14 | ||||
| chr3:184156613-184156798 | Common:1; Rare:41 | ||||
| chr3:184180416-184180644 | Common:2; Rare:62 |