| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7484618-7484834 | Common:1; Rare:94 | ||||
| chr17:7577056-7577385 | Common:1; Rare:86 | ||||
| chr17:7583542-7583858 | Common:1; Rare:130; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:7584073-7584113 | Rare:8 | ||||
| chr17:7627794-7627994 | Common:2; Rare:63 | ||||
| chr17:7686040-7686162 | Rare:46 | ||||
| chr17:7686424-7686688 | Rare:66 | ||||
| chr17:7687476-7687625 | Rare:31 | ||||
| chr17:7688161-7688480 | Common:5; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:7857100-7857320 | Common:1; Rare:111 | ||||
| chr17:7857383-7857634 | Common:2; Rare:87 | ||||
| chr17:7857916-7858100 | Rare:67 | ||||
| chr17:7885176-7885346 | Rare:50 | ||||
| chr17:7885497-7885662 | Rare:34 | ||||
| chr17:7894760-7895036 | Rare:74 |