| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100492757-100492825 | Common:4; Rare:15 | ||||
| chr3:100709234-100709691 | Common:6; Rare:140; Clinvar (benign):1 | ||||
| chr3:101513114-101513319 | Common:8; Rare:42 | ||||
| chr3:101561777-101561915 | Common:1; Rare:44 | ||||
| chr3:101573981-101574225 | Rare:84 | ||||
| chr3:101677092-101677164 | Rare:33 | ||||
| chr3:101686480-101686870 | Common:2; Rare:157 | ||||
| chr3:101724531-101724670 | Rare:51 | ||||
| chr3:101779112-101779253 | Common:3; Rare:45 | ||||
| chr3:105366621-105366935 | Common:3; Rare:85 | ||||
| chr3:105868794-105869193 | Common:7; Rare:135 | ||||
| chr3:107522806-107523082 | Common:1; Rare:65 | ||||
| chr3:108222318-108222569 | Common:2; Rare:69 | ||||
| chr3:108589422-108589561 | Common:2; Rare:30 | ||||
| chr3:108589584-108589754 | Common:1; Rare:54 |