| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33277309-33277501 | Common:1; Rare:53 | ||||
| chr3:33396271-33396461 | Rare:39 | ||||
| chr3:33440362-33440488 | Rare:35 | ||||
| chr3:33718050-33718320 | Rare:105 | ||||
| chr3:33798509-33798934 | Common:3; Rare:153 | ||||
| chr3:33798949-33799073 | Rare:43 | ||||
| chr3:33828313-33828575 | Common:3; Rare:46 | ||||
| chr3:36992372-36992892 | Common:1; Rare:165 | ||||
| chr3:36993020-36993623 | Common:2; Rare:214; Clinvar:40; Clinvar (benign):20; Clinvar (pathogenic):4 | ||||
| chr3:36993709-36993854 | Rare:56; Clinvar:1 | ||||
| chr3:37011846-37012072 | Common:2; Rare:52; Clinvar:11; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr3:37176108-37176401 | Common:1; Rare:80 | ||||
| chr3:37243138-37243512 | Common:3; Rare:105 | ||||
| chr3:37861702-37861805 | Rare:28 | ||||
| chr3:38024506-38024674 | Common:1; Rare:62 |