| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196993-197328 | Common:3; Rare:121 | ||||
| chr3:8501528-8501915 | Common:2; Rare:143 | ||||
| chr3:9362977-9363098 | Common:1; Rare:45 | ||||
| chr3:9749789-9749991 | Rare:63 | ||||
| chr3:9792385-9792592 | Rare:56 | ||||
| chr3:9792726-9793136 | Common:3; Rare:144 | ||||
| chr3:10026289-10026477 | Rare:62 | ||||
| chr3:10115514-10115814 | Common:4; Rare:92 | ||||
| chr3:11643701-11643977 | Rare:67 | ||||
| chr3:12664115-12664324 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:14124716-14125145 | Common:4; Rare:124; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178492-14178866 | Common:3; Rare:182; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14651461-14651786 | Rare:88 | ||||
| chr3:14947223-14947583 | Common:4; Rare:161 | ||||
| chr3:14948324-14948648 | Common:2; Rare:98 |