| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152269514-152269682 | Rare:47 | ||||
| chr3:155854377-155854746 | Rare:103 | ||||
| chr3:156674362-156674618 | Common:3; Rare:73 | ||||
| chr3:157436769-157436993 | Common:2; Rare:52 | ||||
| chr3:158105732-158105874 | Common:5; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158732198-158732250 | Common:2; Rare:20 | ||||
| chr3:160399175-160399309 | Rare:35; Clinvar:2 | ||||
| chr3:160399495-160399656 | Rare:40; Clinvar:1 | ||||
| chr3:160565430-160565868 | Common:2; Rare:156 | ||||
| chr3:167734849-167735074 | Common:2; Rare:76 | ||||
| chr3:167735568-167735745 | Rare:45 | ||||
| chr3:169773319-169773424 | Rare:34 | ||||
| chr3:169966720-169966833 | Rare:50 | ||||
| chr3:174440932-174440982 | Common:1; Rare:16 | ||||
| chr3:179604628-179604816 | Common:1; Rare:58 |