| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4997516-4998292 | Common:12; Rare:475; Clinvar (benign):4 | ||||
| chr17:5191829-5192120 | Common:4; Rare:179 | ||||
| chr17:5282055-5282350 | Common:23; Rare:287 | ||||
| chr17:5419606-5419890 | Common:4; Rare:96 | ||||
| chr17:5420066-5420220 | Rare:112 | ||||
| chr17:5468756-5469135 | Common:3; Rare:142 | ||||
| chr17:5486149-5486608 | Common:10; Rare:308 | ||||
| chr17:5486788-5486933 | Common:8; Rare:83 | ||||
| chr17:5619391-5619555 | Common:2; Rare:97 | ||||
| chr17:6444200-6444457 | Common:4; Rare:137 | ||||
| chr17:6640636-6641199 | Common:15; Rare:311 | ||||
| chr17:6651529-6651821 | Common:2; Rare:187 | ||||
| chr17:6713339-6713642 | Common:3; Rare:67; Clinvar (benign):2 | ||||
| chr17:7012291-7012717 | Rare:279 | ||||
| chr17:7035750-7036151 | Common:1; Rare:178 |