| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142225096-142225123 | Rare:4 | ||||
| chr3:142225300-142225351 | Rare:15 | ||||
| chr3:142225387-142225739 | Common:4; Rare:128 | ||||
| chr3:142447604-142447767 | Common:1; Rare:37 | ||||
| chr3:142447869-142448196 | Common:1; Rare:102 | ||||
| chr3:142578407-142578491 | Rare:18 | ||||
| chr3:142578635-142579090 | Rare:167; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:142596235-142596435 | Common:2; Rare:56 | ||||
| chr3:142723937-142724120 | Common:1; Rare:44 | ||||
| chr3:142724327-142724570 | Common:3; Rare:68 | ||||
| chr3:143001111-143001285 | Rare:29 | ||||
| chr3:143001324-143001656 | Common:5; Rare:111 | ||||
| chr3:143001746-143001871 | Rare:30 | ||||
| chr3:143002201-143002323 | Rare:30 | ||||
| chr3:143118805-143119229 | Common:2; Rare:89 |