| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158110047-158110149 | Rare:21 | ||||
| chr3:158644507-158644698 | Common:5; Rare:71; Clinvar:1; Clinvar (benign):6 | ||||
| chr3:158672369-158672834 | Common:5; Rare:136 | ||||
| chr3:158732141-158732390 | Common:10; Rare:74 | ||||
| chr3:158732455-158732533 | Common:1; Rare:35 | ||||
| chr3:158732642-158732855 | Common:1; Rare:42 | ||||
| chr3:158801950-158802264 | Common:4; Rare:133 | ||||
| chr3:159763606-159763739 | Rare:41 | ||||
| chr3:159763862-159764185 | Common:2; Rare:109 | ||||
| chr3:159764290-159764458 | Common:2; Rare:50 | ||||
| chr3:160399168-160399288 | Rare:27; Clinvar:2 | ||||
| chr3:160399536-160399669 | Rare:28 | ||||
| chr3:160565271-160565901 | Common:3; Rare:204 | ||||
| chr3:160566073-160566234 | Rare:30 | ||||
| chr3:160755452-160755625 | Common:1; Rare:62 |