| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45894278-45894570 | Common:2; Rare:86; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:46192775-46193019 | Common:3; Rare:61; Clinvar (benign):2 | ||||
| chr17:46193293-46193600 | Common:6; Rare:82 | ||||
| chr17:46225347-46225481 | Common:1; Rare:34 | ||||
| chr17:46922827-46923187 | Common:4; Rare:99; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47188816-47188948 | Rare:20 | ||||
| chr17:47189159-47189610 | Common:1; Rare:121 | ||||
| chr17:47323890-47324034 | Common:1; Rare:48 | ||||
| chr17:47530925-47531231 | Common:2; Rare:81 | ||||
| chr17:47591801-47592032 | Common:1; Rare:55 | ||||
| chr17:47649412-47649473 | Rare:13 | ||||
| chr17:47649518-47649980 | Common:1; Rare:168 | ||||
| chr17:47649984-47650284 | Rare:91 | ||||
| chr17:47650304-47650435 | Rare:52 | ||||
| chr17:47820292-47820563 | Rare:58 |