| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127672755-127673043 | Common:6; Rare:136 | ||||
| chr3:127823175-127823340 | Common:3; Rare:32 | ||||
| chr3:128052171-128052569 | Common:2; Rare:133 | ||||
| chr3:128153365-128153531 | Rare:52 | ||||
| chr3:128487920-128488089 | Rare:44 | ||||
| chr3:128726056-128726225 | Common:1; Rare:46; Clinvar:3 | ||||
| chr3:128879421-128879709 | Common:4; Rare:140; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129161004-129161133 | Rare:54 | ||||
| chr3:129183758-129184075 | Common:2; Rare:108 | ||||
| chr3:129249524-129249686 | Common:2; Rare:49 | ||||
| chr3:129278761-129278903 | Common:4; Rare:45 | ||||
| chr3:129316284-129316350 | Rare:23 | ||||
| chr3:129439829-129440382 | Common:1; Rare:167; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129570829-129571067 | Common:2; Rare:81 | ||||
| chr3:129893545-129893875 | Rare:130 |