| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48604027-48604067 | Rare:12 | ||||
| chr17:48604752-48605137 | Common:1; Rare:76 | ||||
| chr17:48605170-48605290 | Common:2; Rare:22 | ||||
| chr17:48610522-48610705 | Common:1; Rare:61 | ||||
| chr17:48610965-48611104 | Common:1; Rare:32 | ||||
| chr17:48614279-48614458 | Rare:66 | ||||
| chr17:48614648-48614909 | Rare:68 | ||||
| chr17:48615097-48615262 | Common:2; Rare:40 | ||||
| chr17:48830907-48831059 | Common:3; Rare:43 | ||||
| chr17:48944773-48944878 | Common:1; Rare:34 | ||||
| chr17:49210438-49210712 | Common:1; Rare:52 | ||||
| chr17:49414834-49415140 | Common:2; Rare:74 | ||||
| chr17:49677950-49678321 | Rare:89 | ||||
| chr17:49788567-49788774 | Common:1; Rare:68 | ||||
| chr17:50188740-50189017 | Rare:72; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):4 |