| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138187211-138187628 | Rare:134 | ||||
| chr3:138187720-138187766 | Rare:13 | ||||
| chr3:138187790-138187828 | Rare:13 | ||||
| chr3:138187957-138188019 | Rare:15 | ||||
| chr3:138594170-138594577 | Rare:123 | ||||
| chr3:138608593-138608994 | Rare:80 | ||||
| chr3:138834419-138834628 | Common:1; Rare:54 | ||||
| chr3:138834809-138835198 | Rare:126 | ||||
| chr3:138835409-138835442 | Rare:5 | ||||
| chr3:139343716-139344109 | Common:1; Rare:118; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:139344196-139344335 | Common:1; Rare:38; Clinvar:1 | ||||
| chr3:139389552-139389936 | Common:2; Rare:122 | ||||
| chr3:140941485-140941939 | Common:3; Rare:146 | ||||
| chr3:140942562-140942740 | Common:1; Rare:55 | ||||
| chr3:141231150-141231360 | Common:2; Rare:43 |