| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:386211-386272 | Common:1; Rare:13 | ||||
| chr17:409989-410453 | Common:9; Rare:212 | ||||
| chr17:522987-523164 | Common:2; Rare:38 | ||||
| chr17:714759-714914 | Common:2; Rare:49 | ||||
| chr17:752143-752379 | Common:3; Rare:95 | ||||
| chr17:752651-752676 | Rare:5 | ||||
| chr17:753997-754305 | Common:3; Rare:70 | ||||
| chr17:864053-864188 | Common:7; Rare:48 | ||||
| chr17:997010-997196 | Common:1; Rare:91 | ||||
| chr17:1078765-1078881 | Common:2; Rare:31 | ||||
| chr17:1400045-1400311 | Common:2; Rare:102 | ||||
| chr17:1400321-1400395 | Common:1; Rare:38 | ||||
| chr17:1400410-1400447 | Rare:9 | ||||
| chr17:1455875-1455976 | Common:2; Rare:27 | ||||
| chr17:1467846-1468052 | Rare:90; Clinvar (benign):3 |