| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37176809-37177015 | Common:4; Rare:43 | ||||
| chr3:37242967-37243616 | Common:5; Rare:184 | ||||
| chr3:37243621-37243760 | Common:2; Rare:62 | ||||
| chr3:37994049-37994260 | Rare:61 | ||||
| chr3:37994275-37994574 | Rare:108 | ||||
| chr3:37998883-37999192 | Common:4; Rare:97 | ||||
| chr3:38024446-38024701 | Common:1; Rare:95 | ||||
| chr3:38024859-38025292 | Common:5; Rare:92 | ||||
| chr3:38136008-38136162 | Common:1; Rare:32 | ||||
| chr3:38136572-38136671 | Rare:30 | ||||
| chr3:38136960-38137623 | Common:1; Rare:171 | ||||
| chr3:38138504-38138800 | Common:2; Rare:103; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:38138930-38139159 | Rare:72; Clinvar (benign):1 | ||||
| chr3:38164656-38164908 | Common:1; Rare:63 | ||||
| chr3:38164910-38165130 | Rare:58 |