| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7548702-7549102 | Common:2; Rare:129 | ||||
| chr17:7561758-7561990 | Common:2; Rare:69 | ||||
| chr17:7572448-7572867 | Common:1; Rare:182 | ||||
| chr17:7583651-7583874 | Common:1; Rare:94; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584074-7584182 | Rare:25 | ||||
| chr17:7614190-7614868 | Common:1; Rare:191 | ||||
| chr17:7614974-7615370 | Rare:116 | ||||
| chr17:7627360-7627710 | Common:1; Rare:112 | ||||
| chr17:7627730-7628040 | Common:3; Rare:99 | ||||
| chr17:7650674-7650932 | Common:2; Rare:71 | ||||
| chr17:7686022-7686178 | Rare:59 | ||||
| chr17:7686387-7686733 | Rare:91 | ||||
| chr17:7687476-7687669 | Rare:39 | ||||
| chr17:7688159-7688502 | Common:5; Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:7704944-7705255 | Common:3; Rare:64 |