| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141431987-141432180 | Common:2; Rare:32 | ||||
| chr3:141738096-141738435 | Common:2; Rare:140 | ||||
| chr3:141738765-141738964 | Common:2; Rare:41 | ||||
| chr3:141876014-141876264 | Rare:69 | ||||
| chr3:141876480-141876682 | Common:1; Rare:76 | ||||
| chr3:141921439-141921602 | Common:1; Rare:26 | ||||
| chr3:142578700-142579003 | Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596279-142596505 | Common:2; Rare:56 | ||||
| chr3:142723908-142724064 | Rare:46 | ||||
| chr3:143001472-143001639 | Common:2; Rare:60 | ||||
| chr3:143971571-143971839 | Common:2; Rare:108 | ||||
| chr3:143971967-143972074 | Rare:42 | ||||
| chr3:143972177-143972293 | Common:1; Rare:36 | ||||
| chr3:146160886-146161293 | Common:1; Rare:138; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146469551-146469810 | Common:5; Rare:61 |