| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35578482-35578702 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:36534852-36535016 | Common:2; Rare:73 | ||||
| chr17:36544809-36544968 | Common:2; Rare:54 | ||||
| chr17:36601491-36601616 | Rare:38 | ||||
| chr17:37406802-37406924 | Rare:48 | ||||
| chr17:37489690-37489919 | Rare:89 | ||||
| chr17:37609351-37609561 | Common:1; Rare:88 | ||||
| chr17:38428270-38428483 | Common:8; Rare:79 | ||||
| chr17:38825264-38825389 | Common:2; Rare:40 | ||||
| chr17:38853696-38853895 | Common:3; Rare:79 | ||||
| chr17:38869902-38870130 | Common:2; Rare:70 | ||||
| chr17:39451242-39451387 | Common:2; Rare:48 | ||||
| chr17:39664906-39665494 | Common:4; Rare:146; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:39688016-39688078 | Rare:23 | ||||
| chr17:39927499-39927745 | Common:2; Rare:74 |