| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:3799840-3800026 | Common:1; Rare:55 | ||||
| chr3:4303202-4303436 | Common:2; Rare:84 | ||||
| chr3:4467201-4467334 | Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493130-4493350 | Common:2; Rare:82 | ||||
| chr3:5187317-5187735 | Common:5; Rare:168 | ||||
| chr3:8501620-8501953 | Common:2; Rare:124 | ||||
| chr3:9249606-9249770 | Common:2; Rare:39 | ||||
| chr3:9362936-9363144 | Common:2; Rare:70 | ||||
| chr3:9397427-9397907 | Common:1; Rare:151 | ||||
| chr3:9553797-9553902 | Rare:28 | ||||
| chr3:9649220-9649547 | Common:1; Rare:113 | ||||
| chr3:9749768-9750144 | Common:1; Rare:112 | ||||
| chr3:9750151-9750380 | Common:1; Rare:86 | ||||
| chr3:9769886-9770057 | Common:1; Rare:43 | ||||
| chr3:9792250-9792583 | Common:1; Rare:88 |