| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42582256-42582304 | Rare:11 | ||||
| chr3:42600353-42600507 | Common:2; Rare:62 | ||||
| chr3:42600579-42601046 | Rare:156 | ||||
| chr3:42630780-42631097 | Common:1; Rare:54 | ||||
| chr3:42633493-42633616 | Rare:31 | ||||
| chr3:42634539-42634675 | Rare:29 | ||||
| chr3:42654120-42654199 | Common:1; Rare:16 | ||||
| chr3:42773211-42773357 | Common:1; Rare:40 | ||||
| chr3:42804266-42804671 | Common:2; Rare:112 | ||||
| chr3:42843692-42844030 | Common:2; Rare:45 | ||||
| chr3:43286431-43286662 | Common:2; Rare:99 | ||||
| chr3:43621894-43622316 | Common:2; Rare:122; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690811-43691016 | Common:4; Rare:114; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:43691553-43691707 | Common:2; Rare:28 | ||||
| chr3:44338375-44338463 | Rare:31 |