| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:88149644-88149764 | Rare:25 | ||||
| chr3:88149823-88150049 | Common:5; Rare:83 | ||||
| chr3:93979904-93980195 | Common:4; Rare:102; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94028639-94028661 | Rare:4 | ||||
| chr3:94062910-94063101 | Rare:43 | ||||
| chr3:97764448-97764821 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821868-97822190 | Common:2; Rare:116 | ||||
| chr3:99638401-99638616 | Common:1; Rare:55 | ||||
| chr3:99817558-99817938 | Rare:118 | ||||
| chr3:99876085-99876308 | Common:2; Rare:64 | ||||
| chr3:100260715-100261054 | Rare:99 | ||||
| chr3:100261336-100261599 | Common:1; Rare:54 | ||||
| chr3:100401407-100401580 | Common:1; Rare:30 | ||||
| chr3:100492431-100492674 | Common:2; Rare:79 | ||||
| chr3:100709234-100709686 | Common:6; Rare:139; Clinvar (benign):1 |