| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:150603162-150603360 | Common:2; Rare:79 | ||||
| chr3:152268646-152269153 | Rare:187 | ||||
| chr3:152269533-152269682 | Rare:39 | ||||
| chr3:155870323-155870700 | Common:2; Rare:113 | ||||
| chr3:156555052-156555338 | Common:1; Rare:120 | ||||
| chr3:156674373-156674647 | Common:3; Rare:78 | ||||
| chr3:157160076-157160343 | Rare:107 | ||||
| chr3:158105739-158105906 | Common:5; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158110061-158110168 | Rare:22 | ||||
| chr3:158801997-158802146 | Common:2; Rare:72 | ||||
| chr3:159763170-159763340 | Rare:30 | ||||
| chr3:160399196-160399290 | Rare:22; Clinvar:1 | ||||
| chr3:160399547-160399669 | Rare:26 | ||||
| chr3:160449706-160450038 | Common:2; Rare:115 | ||||
| chr3:160450190-160450409 | Common:2; Rare:61 |