| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3668552-3668828 | Common:2; Rare:107 | ||||
| chr17:3723767-3723925 | Common:1; Rare:89 | ||||
| chr17:3892983-3893239 | Common:2; Rare:88 | ||||
| chr17:4143001-4143239 | Rare:78 | ||||
| chr17:4143597-4143740 | Common:4; Rare:80 | ||||
| chr17:4263943-4264024 | Rare:35 | ||||
| chr17:4704100-4704271 | Rare:84 | ||||
| chr17:4739382-4739647 | Common:5; Rare:65 | ||||
| chr17:4807014-4807210 | Common:4; Rare:62 | ||||
| chr17:4899383-4899460 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:4939887-4940341 | Common:2; Rare:136 | ||||
| chr17:4948942-4949110 | Common:1; Rare:57 | ||||
| chr17:4967781-4967846 | Rare:30 | ||||
| chr17:4987625-4987753 | Common:1; Rare:52 | ||||
| chr17:4997892-4998006 | Common:1; Rare:43 |