| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76354196-76354286 | Rare:20 | ||||
| chr17:76726443-76726904 | Common:5; Rare:177 | ||||
| chr17:76737325-76737691 | Common:3; Rare:125 | ||||
| chr17:76737877-76738121 | Common:4; Rare:70 | ||||
| chr17:77088579-77088787 | Common:1; Rare:57 | ||||
| chr17:77140542-77141034 | Common:5; Rare:171 | ||||
| chr17:78041204-78041272 | Rare:13 | ||||
| chr17:78168456-78168611 | Rare:41 | ||||
| chr17:78187018-78187411 | Common:3; Rare:142 | ||||
| chr17:78214066-78214353 | Common:5; Rare:96 | ||||
| chr17:78378516-78378680 | Rare:55 | ||||
| chr17:78782233-78782553 | Common:8; Rare:104 | ||||
| chr17:78840745-78841096 | Common:2; Rare:133 | ||||
| chr17:78979889-78980052 | Common:2; Rare:37 | ||||
| chr17:79009732-79009935 | Common:8; Rare:60; Clinvar:1; Clinvar (benign):1 |