| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47189187-47189422 | Common:1; Rare:70 | ||||
| chr17:47323868-47324025 | Common:1; Rare:58 | ||||
| chr17:47831501-47831646 | Rare:39 | ||||
| chr17:47941356-47941702 | Rare:93; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048619-48048833 | Common:3; Rare:34 | ||||
| chr17:48107412-48107617 | Common:4; Rare:52 | ||||
| chr17:48107681-48107784 | Common:1; Rare:25 | ||||
| chr17:48544588-48544640 | Rare:24 | ||||
| chr17:48610522-48610705 | Common:1; Rare:61 | ||||
| chr17:48614279-48614299 | Rare:4 | ||||
| chr17:48625852-48626149 | Rare:106 | ||||
| chr17:48944708-48944909 | Common:2; Rare:70 | ||||
| chr17:48997125-48997518 | Rare:79 | ||||
| chr17:49210182-49210436 | Common:2; Rare:40 | ||||
| chr17:49210591-49210721 | Rare:21 |