| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138608739-138609091 | Rare:83 | ||||
| chr3:138834874-138835087 | Rare:76 | ||||
| chr3:139344221-139344621 | Common:1; Rare:83 | ||||
| chr3:139389568-139389869 | Common:1; Rare:97 | ||||
| chr3:139539543-139539743 | Common:3; Rare:74 | ||||
| chr3:140941532-140941939 | Common:3; Rare:136 | ||||
| chr3:141231688-141231888 | Common:1; Rare:69 | ||||
| chr3:142225491-142225634 | Common:3; Rare:51 | ||||
| chr3:142447968-142448153 | Common:1; Rare:72 | ||||
| chr3:142578690-142578963 | Rare:104; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596249-142596459 | Common:2; Rare:58 | ||||
| chr3:143001209-143001631 | Common:5; Rare:113 | ||||
| chr3:146160967-146161267 | Common:1; Rare:101; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146544545-146544792 | Common:3; Rare:59 | ||||
| chr3:148991383-148991620 | Common:2; Rare:111; Clinvar (benign):1 |