| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138608966-138609115 | Common:1; Rare:46 | ||||
| chr3:139389568-139389878 | Common:2; Rare:98 | ||||
| chr3:139539569-139539589 | Common:1; Rare:8 | ||||
| chr3:139539592-139539788 | Common:1; Rare:59 | ||||
| chr3:140941655-140941939 | Common:2; Rare:103 | ||||
| chr3:140942092-140942213 | Common:2; Rare:31 | ||||
| chr3:141368260-141368353 | Rare:21 | ||||
| chr3:141368422-141368540 | Rare:23 | ||||
| chr3:141876036-141876246 | Rare:61 | ||||
| chr3:142578699-142578915 | Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142723830-142724050 | Rare:56 | ||||
| chr3:143001427-143001626 | Common:3; Rare:73 | ||||
| chr3:143971673-143971837 | Common:1; Rare:82 | ||||
| chr3:146160991-146161320 | Common:2; Rare:106; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146251010-146251364 | Common:2; Rare:92 |