| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19377446-19377765 | Common:2; Rare:72 | ||||
| chr17:19377898-19378028 | Common:1; Rare:32 | ||||
| chr17:19378162-19378545 | Common:2; Rare:92 | ||||
| chr17:19648590-19648992 | Common:4; Rare:139 | ||||
| chr17:19977816-19977958 | Common:1; Rare:47 | ||||
| chr17:20009192-20009383 | Common:2; Rare:60 | ||||
| chr17:20155851-20156146 | Common:1; Rare:97 | ||||
| chr17:20868223-20868543 | Common:3; Rare:76 | ||||
| chr17:21042234-21042436 | Common:1; Rare:78 | ||||
| chr17:21043400-21043506 | Rare:41 | ||||
| chr17:21214140-21214351 | Common:2; Rare:94 | ||||
| chr17:27293903-27294120 | Common:1; Rare:88 | ||||
| chr17:28318932-28319323 | Common:3; Rare:141 | ||||
| chr17:28335421-28335832 | Common:1; Rare:95 | ||||
| chr17:28357444-28357703 | Common:5; Rare:130; Clinvar (pathogenic):1 |