| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5191833-5192112 | Common:2; Rare:89 | ||||
| chr17:5234802-5234976 | Rare:39 | ||||
| chr17:5282081-5282292 | Common:9; Rare:105 | ||||
| chr17:5419556-5419882 | Common:3; Rare:114 | ||||
| chr17:5420053-5420213 | Rare:64 | ||||
| chr17:5438887-5439198 | Common:1; Rare:116 | ||||
| chr17:5486157-5486581 | Common:5; Rare:143 | ||||
| chr17:5486800-5486917 | Common:4; Rare:34 | ||||
| chr17:6444140-6444435 | Common:2; Rare:87 | ||||
| chr17:6640645-6641090 | Common:7; Rare:140 | ||||
| chr17:6651553-6651721 | Common:1; Rare:63 | ||||
| chr17:6755902-6756081 | Common:3; Rare:46 | ||||
| chr17:7012297-7012726 | Rare:140 | ||||
| chr17:7035817-7036026 | Rare:51 | ||||
| chr17:7219728-7219956 | Common:3; Rare:90; Clinvar:5; Clinvar (benign):2 |