| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100334550-100334786 | Common:2; Rare:79 | ||||
| chr3:100401064-100401197 | Rare:38 | ||||
| chr3:100401398-100401592 | Common:1; Rare:36 | ||||
| chr3:100492420-100492801 | Common:11; Rare:108 | ||||
| chr3:100709207-100709721 | Common:9; Rare:155; Clinvar (benign):1 | ||||
| chr3:101513103-101513319 | Common:8; Rare:47 | ||||
| chr3:101561740-101561931 | Common:2; Rare:66 | ||||
| chr3:101573981-101574300 | Common:1; Rare:112 | ||||
| chr3:101677074-101677171 | Rare:43 | ||||
| chr3:101686480-101686870 | Common:2; Rare:157 | ||||
| chr3:101724558-101724650 | Rare:33 | ||||
| chr3:101779127-101779273 | Common:4; Rare:51 | ||||
| chr3:101779379-101779670 | Common:2; Rare:75 | ||||
| chr3:105366422-105366771 | Common:3; Rare:93 | ||||
| chr3:105366822-105366935 | Common:1; Rare:25 |