| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:16465694-16465895 | Rare:40 | ||||
| chr5:16616973-16617225 | Common:2; Rare:74; Clinvar (benign):5 | ||||
| chr5:31532037-31532346 | Common:3; Rare:86 | ||||
| chr5:31854764-31854992 | Common:1; Rare:73 | ||||
| chr5:32174243-32174437 | Common:2; Rare:73 | ||||
| chr5:32711012-32711276 | Common:1; Rare:46 | ||||
| chr5:32712187-32712366 | Rare:52 | ||||
| chr5:33440606-33441095 | Common:7; Rare:132 | ||||
| chr5:33891976-33892279 | Rare:65 | ||||
| chr5:34656158-34656501 | Common:3; Rare:84 | ||||
| chr5:34915216-34915279 | Rare:18 | ||||
| chr5:34929590-34929915 | Rare:111 | ||||
| chr5:35856767-35856926 | Rare:24 | ||||
| chr5:36151830-36152153 | Rare:83 | ||||
| chr5:36606543-36606735 | Rare:34 |