| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17836193-17836635 | Common:3; Rare:114 | ||||
| chr17:17836909-17837071 | Common:2; Rare:35 | ||||
| chr17:18039100-18039469 | Common:5; Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18087747-18088018 | Rare:74 | ||||
| chr17:18182843-18183152 | Common:1; Rare:85 | ||||
| chr17:18183188-18183561 | Rare:103 | ||||
| chr17:18183765-18183978 | Rare:99 | ||||
| chr17:18257942-18258084 | Rare:27 | ||||
| chr17:18258143-18258265 | Rare:29 | ||||
| chr17:18258395-18258612 | Common:3; Rare:58 | ||||
| chr17:18258682-18258868 | Common:1; Rare:47 | ||||
| chr17:18258946-18259087 | Common:1; Rare:30 | ||||
| chr17:18260406-18260691 | Rare:83 | ||||
| chr17:18260765-18260997 | Common:3; Rare:61 | ||||
| chr17:18261258-18261393 | Common:3; Rare:25 |