| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7438183-7438329 | Rare:34 | ||||
| chr17:7479490-7479740 | Common:1; Rare:44 | ||||
| chr17:7484231-7484371 | Common:1; Rare:57 | ||||
| chr17:7484690-7484844 | Rare:61 | ||||
| chr17:7583535-7583858 | Common:1; Rare:131; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:7584073-7584102 | Rare:6 | ||||
| chr17:7627664-7627996 | Common:3; Rare:114 | ||||
| chr17:7686402-7686677 | Rare:69 | ||||
| chr17:7687476-7687569 | Rare:24 | ||||
| chr17:7854853-7855148 | Common:1; Rare:111 | ||||
| chr17:7857100-7857296 | Common:1; Rare:95 | ||||
| chr17:7857382-7857718 | Common:3; Rare:108 | ||||
| chr17:7857854-7858100 | Rare:88 | ||||
| chr17:7885200-7885346 | Rare:42 | ||||
| chr17:7931910-7932259 | Common:5; Rare:96 |