| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44218221-44218378 | Rare:36 | ||||
| chr17:44219465-44219821 | Rare:131 | ||||
| chr17:44220830-44221019 | Rare:57 | ||||
| chr17:44221273-44221412 | Rare:41 | ||||
| chr17:44324735-44325013 | Common:3; Rare:102 | ||||
| chr17:44503359-44503632 | Rare:114 | ||||
| chr17:44557209-44557457 | Common:2; Rare:47 | ||||
| chr17:44708519-44708746 | Common:1; Rare:48 | ||||
| chr17:44899371-44899800 | Common:3; Rare:131; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:45051405-45051690 | Common:1; Rare:93 | ||||
| chr17:45060909-45061458 | Common:3; Rare:157 | ||||
| chr17:45132514-45132666 | Common:1; Rare:56 | ||||
| chr17:45148233-45149122 | Common:5; Rare:284 | ||||
| chr17:45161507-45161643 | Rare:42 | ||||
| chr17:45221460-45221807 | Common:1; Rare:89 |