| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44066597-44066811 | Common:1; Rare:84 | ||||
| chr17:44070548-44071031 | Common:3; Rare:156; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:44086760-44087250 | Common:4; Rare:135 | ||||
| chr17:44111120-44111440 | Common:1; Rare:98 | ||||
| chr17:44123594-44123912 | Common:3; Rare:92 | ||||
| chr17:44142433-44142579 | Common:1; Rare:34 | ||||
| chr17:44186634-44187021 | Common:1; Rare:137 | ||||
| chr17:44198240-44198640 | Common:5; Rare:127 | ||||
| chr17:44200075-44200372 | Common:2; Rare:120 | ||||
| chr17:44218078-44218486 | Common:1; Rare:191 | ||||
| chr17:44218500-44218809 | Rare:103 | ||||
| chr17:44219920-44220116 | Common:4; Rare:57 | ||||
| chr17:44220830-44220934 | Rare:22 | ||||
| chr17:44221275-44221427 | Rare:45 | ||||
| chr17:44307930-44308180 | Rare:32 |