| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138834844-138834995 | Rare:46 | ||||
| chr3:139389567-139389820 | Common:1; Rare:81 | ||||
| chr3:140941618-140941873 | Common:2; Rare:92 | ||||
| chr3:141368441-141368539 | Rare:19 | ||||
| chr3:141738179-141738516 | Rare:114 | ||||
| chr3:142888895-142889042 | Common:3; Rare:42 | ||||
| chr3:143001367-143001634 | Common:4; Rare:93 | ||||
| chr3:146160890-146161190 | Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:149377460-149377863 | Common:1; Rare:112 | ||||
| chr3:150603168-150603321 | Common:1; Rare:57 | ||||
| chr3:152269540-152269659 | Rare:36 | ||||
| chr3:156555008-156555333 | Common:1; Rare:132 | ||||
| chr3:156674362-156674618 | Common:3; Rare:73 | ||||
| chr3:157149284-157149513 | Rare:58 | ||||
| chr3:158105728-158105878 | Common:5; Rare:78; Clinvar:2; Clinvar (benign):1 |