| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44141791-44142000 | Common:1; Rare:53 | ||||
| chr17:44186614-44187037 | Common:1; Rare:146 | ||||
| chr17:44187178-44187425 | Common:1; Rare:57 | ||||
| chr17:44198198-44198545 | Common:3; Rare:69 | ||||
| chr17:44210389-44210677 | Rare:121 | ||||
| chr17:44219185-44219227 | Rare:12 | ||||
| chr17:44220478-44220652 | Common:3; Rare:71 | ||||
| chr17:44220825-44220971 | Rare:42 | ||||
| chr17:44221200-44221390 | Rare:52 | ||||
| chr17:44222103-44222321 | Rare:44 | ||||
| chr17:44268093-44268376 | Rare:59; Clinvar:3 | ||||
| chr17:44324765-44325005 | Common:2; Rare:86 | ||||
| chr17:44350438-44350801 | Rare:126; Clinvar:9; Clinvar (benign):5 | ||||
| chr17:44503352-44503714 | Rare:137 | ||||
| chr17:44899367-44899748 | Common:2; Rare:119; Clinvar:2; Clinvar (benign):1 |