| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100492083-100492219 | Rare:37 | ||||
| chr3:100492413-100492658 | Common:2; Rare:83 | ||||
| chr3:100709235-100709628 | Common:6; Rare:128; Clinvar (benign):1 | ||||
| chr3:101513126-101513341 | Common:8; Rare:45 | ||||
| chr3:101561743-101561915 | Common:1; Rare:60 | ||||
| chr3:101573981-101574233 | Rare:87 | ||||
| chr3:101677090-101677391 | Rare:100 | ||||
| chr3:101686663-101686860 | Common:2; Rare:83 | ||||
| chr3:101724531-101724650 | Rare:43 | ||||
| chr3:105868885-105869186 | Common:6; Rare:109 | ||||
| chr3:108222306-108222638 | Common:3; Rare:100 | ||||
| chr3:108589379-108589745 | Common:3; Rare:120 | ||||
| chr3:109337465-109337737 | Common:2; Rare:91 | ||||
| chr3:111674475-111674750 | Rare:97 | ||||
| chr3:111978912-111979064 | Common:1; Rare:53 |