| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4533808-4534086 | Rare:57 | ||||
| chr3:4580754-4580887 | Rare:31 | ||||
| chr3:4625325-4625536 | Common:1; Rare:36 | ||||
| chr3:4687002-4688150 | Common:19; Rare:408 | ||||
| chr3:4688402-4688820 | Rare:101; Clinvar (benign):1 | ||||
| chr3:4695820-4696360 | Common:6; Rare:194 | ||||
| chr3:4713990-4714397 | Common:22; Rare:253 | ||||
| chr3:4714530-4715173 | Common:8; Rare:146 | ||||
| chr3:4719021-4719230 | Rare:44 | ||||
| chr3:4720205-4720605 | Common:6; Rare:167 | ||||
| chr3:4750210-4750630 | Common:1; Rare:86 | ||||
| chr3:4776582-4777505 | Common:3; Rare:321 | ||||
| chr3:4847837-4848606 | Common:5; Rare:249 | ||||
| chr3:4868230-4869000 | Common:6; Rare:608 | ||||
| chr3:4977410-4977950 | Common:4; Rare:127 |