| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:18184736-18184957 | Common:1; Rare:49 | ||||
| chr17:18247011-18247358 | Common:8; Rare:174 | ||||
| chr17:18247399-18247429 | Rare:9 | ||||
| chr17:18253374-18253682 | Rare:113 | ||||
| chr17:18254519-18254823 | Rare:104 | ||||
| chr17:18258683-18259013 | Common:1; Rare:75 | ||||
| chr17:18314921-18315359 | Common:1; Rare:125 | ||||
| chr17:18377523-18377787 | Common:2; Rare:64 | ||||
| chr17:18781091-18781305 | Common:5; Rare:59 | ||||
| chr17:18856169-18856362 | Common:1; Rare:34 | ||||
| chr17:19004117-19004317 | Rare:49 | ||||
| chr17:19004726-19004878 | Common:1; Rare:52 | ||||
| chr17:19257608-19257611 | Rare:1 | ||||
| chr17:19362674-19362748 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chr17:19377632-19377788 | Common:2; Rare:41 |