| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:38749779-38749906 | Rare:32 | ||||
| chr17:38752518-38752829 | Common:4; Rare:88 | ||||
| chr17:38825278-38825427 | Common:2; Rare:45 | ||||
| chr17:38853679-38853895 | Common:3; Rare:84 | ||||
| chr17:38869873-38870189 | Common:4; Rare:103 | ||||
| chr17:39199982-39200349 | Common:3; Rare:114 | ||||
| chr17:39203881-39204113 | Rare:48 | ||||
| chr17:39401609-39401816 | Common:1; Rare:56 | ||||
| chr17:39451249-39451394 | Common:2; Rare:48 | ||||
| chr17:39461329-39461539 | Common:1; Rare:62 | ||||
| chr17:39637052-39637198 | Common:3; Rare:47 | ||||
| chr17:39664885-39665170 | Common:2; Rare:56 | ||||
| chr17:39665196-39665478 | Common:1; Rare:84; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:39688016-39688132 | Rare:39 | ||||
| chr17:39699894-39700240 | Rare:90 |