| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4997900-4998154 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr17:5007319-5007536 | Rare:65 | ||||
| chr17:5078365-5078536 | Common:4; Rare:52 | ||||
| chr17:5123099-5123420 | Rare:107 | ||||
| chr17:5191826-5192130 | Common:2; Rare:99 | ||||
| chr17:5234804-5234946 | Rare:35 | ||||
| chr17:5419585-5420287 | Common:6; Rare:241 | ||||
| chr17:5438150-5438478 | Common:1; Rare:77 | ||||
| chr17:5486143-5486608 | Common:5; Rare:159 | ||||
| chr17:5486796-5486926 | Common:4; Rare:41 | ||||
| chr17:6640641-6641085 | Common:7; Rare:136 | ||||
| chr17:6651574-6651767 | Common:1; Rare:62 | ||||
| chr17:6755878-6756110 | Common:3; Rare:59 | ||||
| chr17:6831683-6831778 | Rare:12 | ||||
| chr17:6995980-6996049 | Rare:19 |