| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43833114-43833294 | Common:1; Rare:52 | ||||
| chr17:44123596-44123828 | Common:3; Rare:69 | ||||
| chr17:44186673-44187003 | Common:1; Rare:116 | ||||
| chr17:44187171-44187274 | Rare:29 | ||||
| chr17:44324765-44324946 | Common:1; Rare:67 | ||||
| chr17:44503377-44503713 | Rare:132 | ||||
| chr17:44899375-44899778 | Common:3; Rare:127; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:45061069-45061389 | Common:1; Rare:105 | ||||
| chr17:45132370-45132639 | Common:1; Rare:83 | ||||
| chr17:45148165-45148602 | Common:1; Rare:152 | ||||
| chr17:45161494-45161895 | Common:1; Rare:107 | ||||
| chr17:45490708-45490873 | Rare:56 | ||||
| chr17:46192823-46193020 | Common:1; Rare:50 | ||||
| chr17:46923071-46923174 | Common:1; Rare:43; Clinvar (benign):6 | ||||
| chr17:47189246-47189568 | Rare:82 |