| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:156816968-156817330 | Rare:109 | ||||
| chr3:157156495-157156584 | Rare:18 | ||||
| chr3:157456636-157456906 | Common:4; Rare:52 | ||||
| chr3:158659707-158659751 | Rare:3 | ||||
| chr3:158666378-158666437 | Common:2; Rare:21; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:158666728-158667059 | Common:1; Rare:64 | ||||
| chr3:159732213-159732392 | Common:1; Rare:35 | ||||
| chr3:159877482-159877722 | Common:2; Rare:42 | ||||
| chr3:160423548-160423803 | Rare:76 | ||||
| chr3:160447599-160447774 | Common:1; Rare:24 | ||||
| chr3:160515198-160515577 | Common:1; Rare:71 | ||||
| chr3:160566089-160566576 | Common:1; Rare:89 | ||||
| chr3:160566670-160566877 | Common:3; Rare:37 | ||||
| chr3:161254021-161254109 | Rare:15 | ||||
| chr3:168096503-168096587 | Rare:13 |