| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100709229-100709716 | Common:6; Rare:148; Clinvar (benign):1 | ||||
| chr3:100993309-100993594 | Common:3; Rare:59 | ||||
| chr3:101513122-101513358 | Common:8; Rare:57 | ||||
| chr3:101561777-101561979 | Common:2; Rare:71 | ||||
| chr3:101574007-101574277 | Common:1; Rare:98 | ||||
| chr3:101677070-101677171 | Rare:44 | ||||
| chr3:101685816-101686104 | Common:4; Rare:71 | ||||
| chr3:101686661-101686819 | Common:2; Rare:72 | ||||
| chr3:101724562-101724654 | Rare:36 | ||||
| chr3:101779078-101779253 | Common:4; Rare:53 | ||||
| chr3:101779346-101779686 | Common:2; Rare:87 | ||||
| chr3:105366882-105366914 | Rare:8 | ||||
| chr3:105367167-105367311 | Common:1; Rare:36 | ||||
| chr3:105868754-105869186 | Common:7; Rare:141 | ||||
| chr3:108222314-108222631 | Common:3; Rare:97 |