| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129278777-129278900 | Common:3; Rare:33 | ||||
| chr3:129439843-129440350 | Common:1; Rare:156; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893580-129893882 | Rare:129 | ||||
| chr3:130746796-130746913 | Common:3; Rare:37 | ||||
| chr3:130893914-130894242 | Common:3; Rare:94 | ||||
| chr3:131026740-131026951 | Common:2; Rare:53 | ||||
| chr3:131381462-131381811 | Common:3; Rare:89 | ||||
| chr3:131502814-131502995 | Common:1; Rare:86 | ||||
| chr3:132417171-132417662 | Common:6; Rare:168 | ||||
| chr3:132659799-132659942 | Common:3; Rare:33 | ||||
| chr3:133661863-133662033 | Rare:40 | ||||
| chr3:134485670-134485766 | Rare:36 | ||||
| chr3:134485950-134486253 | Common:4; Rare:109 | ||||
| chr3:136752341-136752644 | Common:1; Rare:90 | ||||
| chr3:136819044-136819181 | Common:3; Rare:88 |