| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:13601967-13602159 | Common:1; Rare:61 | ||||
| chr17:14069430-14069539 | Common:1; Rare:39; Clinvar (benign):2 | ||||
| chr17:15999568-15999863 | Common:3; Rare:153; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:16215378-16215643 | Common:2; Rare:105 | ||||
| chr17:17281194-17281392 | Rare:79 | ||||
| chr17:18039081-18039430 | Common:5; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18314921-18315339 | Common:1; Rare:121 | ||||
| chr17:18856204-18856362 | Common:1; Rare:26 | ||||
| chr17:19004154-19004410 | Common:1; Rare:55 | ||||
| chr17:19377619-19377793 | Common:2; Rare:44 | ||||
| chr17:19377905-19378029 | Common:1; Rare:29 | ||||
| chr17:19378156-19378572 | Common:2; Rare:100 | ||||
| chr17:21042966-21043295 | Common:4; Rare:122 | ||||
| chr17:21214092-21214368 | Common:2; Rare:128 | ||||
| chr17:28042227-28042536 | Common:2; Rare:77 |