| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4966897-4967250 | Common:3; Rare:88 | ||||
| chr17:4967256-4967630 | Common:2; Rare:108 | ||||
| chr17:4967740-4967976 | Rare:97 | ||||
| chr17:4987431-4987761 | Common:3; Rare:108 | ||||
| chr17:4997884-4998146 | Common:2; Rare:104; Clinvar (benign):1 | ||||
| chr17:5191838-5192123 | Common:2; Rare:91 | ||||
| chr17:5282077-5282292 | Common:9; Rare:108 | ||||
| chr17:5419591-5420015 | Common:6; Rare:127 | ||||
| chr17:5420122-5420214 | Rare:38 | ||||
| chr17:5438887-5439002 | Rare:37 | ||||
| chr17:5486140-5486630 | Common:5; Rare:168 | ||||
| chr17:5486805-5486938 | Common:4; Rare:40 | ||||
| chr17:5500988-5501260 | Common:3; Rare:82 | ||||
| chr17:6640638-6641097 | Common:7; Rare:143 | ||||
| chr17:6651524-6651748 | Common:1; Rare:76 |