| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:155853618-155853841 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:155854311-155854892 | Common:1; Rare:151; Clinvar (benign):1 | ||||
| chr3:155870213-155870744 | Common:2; Rare:146 | ||||
| chr3:156555045-156555432 | Common:2; Rare:144 | ||||
| chr3:156674314-156674685 | Common:5; Rare:105 | ||||
| chr3:156675584-156675667 | Common:1; Rare:19 | ||||
| chr3:156825955-156826048 | Common:1; Rare:25 | ||||
| chr3:156826053-156826672 | Common:3; Rare:159 | ||||
| chr3:157159251-157159575 | Common:6; Rare:110 | ||||
| chr3:157160028-157160544 | Common:1; Rare:180 | ||||
| chr3:157160699-157160930 | Common:5; Rare:53 | ||||
| chr3:158109996-158110216 | Rare:52 | ||||
| chr3:158110265-158110497 | Common:2; Rare:63 | ||||
| chr3:158644355-158644670 | Common:5; Rare:102; Clinvar (benign):6 | ||||
| chr3:158644751-158644858 | Common:1; Rare:28 |