| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138834862-138835028 | Rare:53 | ||||
| chr3:139389568-139389875 | Common:2; Rare:98 | ||||
| chr3:139539581-139539788 | Common:1; Rare:67 | ||||
| chr3:140941672-140941962 | Common:2; Rare:101 | ||||
| chr3:141231652-141231888 | Common:2; Rare:83 | ||||
| chr3:141323939-141324239 | Common:1; Rare:41 | ||||
| chr3:141324257-141324416 | Rare:25 | ||||
| chr3:141368260-141368540 | Rare:58 | ||||
| chr3:141402046-141402431 | Common:2; Rare:93 | ||||
| chr3:141738700-141739034 | Common:2; Rare:69 | ||||
| chr3:141876069-141876246 | Rare:50 | ||||
| chr3:141876452-141876729 | Common:2; Rare:101 | ||||
| chr3:142578700-142579003 | Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596068-142596131 | Rare:10 | ||||
| chr3:142596264-142596516 | Common:3; Rare:62 |