| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5468933-5469105 | Common:2; Rare:57 | ||||
| chr17:6640660-6641226 | Common:8; Rare:193 | ||||
| chr17:6651566-6651712 | Common:1; Rare:55 | ||||
| chr17:7012301-7012684 | Rare:132 | ||||
| chr17:7219817-7219976 | Common:3; Rare:75; Clinvar:6; Clinvar (benign):2 | ||||
| chr17:7241784-7241951 | Common:2; Rare:36 | ||||
| chr17:7242291-7242626 | Common:1; Rare:109 | ||||
| chr17:7251931-7252595 | Common:4; Rare:251 | ||||
| chr17:7307470-7308093 | Common:4; Rare:165 | ||||
| chr17:7479507-7479761 | Common:1; Rare:44 | ||||
| chr17:7484127-7484371 | Common:1; Rare:84 | ||||
| chr17:7561788-7562095 | Common:3; Rare:82 | ||||
| chr17:7583515-7583889 | Common:1; Rare:150; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7584057-7584309 | Common:1; Rare:61 | ||||
| chr17:7687377-7687431 | Rare:9; Clinvar:1 |