| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:188154081-188154219 | Rare:44 | ||||
| chr3:188212346-188212696 | Common:1; Rare:50 | ||||
| chr3:189631096-189631422 | Common:3; Rare:61 | ||||
| chr3:190120262-190120680 | Common:1; Rare:178; Clinvar (pathogenic):1 | ||||
| chr3:190120800-190121132 | Rare:92 | ||||
| chr3:190322036-190322098 | Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:190322330-190322543 | Common:2; Rare:55 | ||||
| chr3:192917824-192918024 | Common:2; Rare:88 | ||||
| chr3:193593069-193593399 | Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194136077-194136328 | Common:2; Rare:60 | ||||
| chr3:194633602-194633792 | Common:3; Rare:39 | ||||
| chr3:194650878-194651206 | Common:2; Rare:91 | ||||
| chr3:195271089-195271350 | Common:2; Rare:105 | ||||
| chr3:195542905-195542951 | Rare:16 | ||||
| chr3:195895911-195895990 | Rare:32 |