| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:99638459-99638630 | Common:1; Rare:39 | ||||
| chr3:99817543-99817924 | Rare:115 | ||||
| chr3:99876124-99876324 | Common:1; Rare:55 | ||||
| chr3:100260706-100261024 | Rare:85 | ||||
| chr3:100401398-100401580 | Common:1; Rare:34 | ||||
| chr3:100492413-100492785 | Common:11; Rare:112 | ||||
| chr3:100709234-100709559 | Common:5; Rare:113; Clinvar (benign):1 | ||||
| chr3:101561743-101561931 | Common:2; Rare:66 | ||||
| chr3:101574049-101574253 | Rare:71 | ||||
| chr3:101677065-101677171 | Rare:45 | ||||
| chr3:101685816-101686127 | Common:4; Rare:81 | ||||
| chr3:101686480-101686880 | Common:2; Rare:160 | ||||
| chr3:101724530-101724642 | Rare:38 | ||||
| chr3:105366623-105366919 | Common:3; Rare:77 | ||||
| chr3:105367154-105367264 | Common:1; Rare:27 |