| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15999586-16000177 | Common:4; Rare:246; Clinvar:6; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr17:16215532-16215686 | Common:1; Rare:69 | ||||
| chr17:16217094-16217259 | Rare:60; Clinvar:2 | ||||
| chr17:16344519-16344608 | Common:1; Rare:22 | ||||
| chr17:16380697-16380814 | Common:1; Rare:24 | ||||
| chr17:16415516-16415798 | Common:4; Rare:74 | ||||
| chr17:17237133-17237699 | Common:8; Rare:152; Clinvar (benign):2 | ||||
| chr17:17280694-17280864 | Common:3; Rare:62 | ||||
| chr17:17281164-17281392 | Rare:88 | ||||
| chr17:17476886-17477102 | Common:3; Rare:72 | ||||
| chr17:17591361-17591504 | Common:1; Rare:50 | ||||
| chr17:17591573-17591939 | Common:2; Rare:107 | ||||
| chr17:17592081-17592306 | Common:1; Rare:70 | ||||
| chr17:17823542-17823974 | Common:6; Rare:170 | ||||
| chr17:17836783-17837084 | Common:3; Rare:71 |