| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1736320-1736750 | Common:9; Rare:170 | ||||
| chr17:1995496-1995612 | Common:1; Rare:31 | ||||
| chr17:2049880-2050120 | Common:2; Rare:88 | ||||
| chr17:2398860-2399130 | Common:1; Rare:65 | ||||
| chr17:2399484-2399908 | Common:6; Rare:313 | ||||
| chr17:3794728-3795128 | Common:4; Rare:194 | ||||
| chr17:4003780-4004180 | Common:2; Rare:83 | ||||
| chr17:4014435-4014587 | Rare:40 | ||||
| chr17:4778301-4778761 | Common:3; Rare:153 | ||||
| chr17:4834130-4834469 | Common:6; Rare:110 | ||||
| chr17:4880701-4881370 | Common:5; Rare:210 | ||||
| chr17:4908229-4908851 | Common:22; Rare:162 | ||||
| chr17:4998920-4999430 | Common:10; Rare:182 | ||||
| chr17:6677120-6677380 | Common:5; Rare:55 | ||||
| chr17:6700607-6701260 | Common:1; Rare:290; Clinvar:6; Clinvar (benign):15 |