| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44899369-44899736 | Common:2; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:45060987-45061339 | Common:2; Rare:93 | ||||
| chr17:45148149-45148476 | Common:1; Rare:92 | ||||
| chr17:45161494-45161845 | Common:1; Rare:90 | ||||
| chr17:45490713-45490863 | Rare:52 | ||||
| chr17:47189235-47189616 | Rare:97 | ||||
| chr17:47323862-47323962 | Common:1; Rare:38 | ||||
| chr17:47941368-47941601 | Rare:48; Clinvar:1 | ||||
| chr17:48048069-48048446 | Rare:101 | ||||
| chr17:48107462-48107760 | Common:5; Rare:67 | ||||
| chr17:48590239-48590420 | Common:1; Rare:40 | ||||
| chr17:48604960-48605130 | Common:1; Rare:30 | ||||
| chr17:48722504-48722667 | Rare:31 | ||||
| chr17:48722968-48723194 | Rare:48 | ||||
| chr17:48729047-48729290 | Rare:52 |