| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19378120-19378549 | Common:2; Rare:104 | ||||
| chr17:19387151-19387385 | Rare:58 | ||||
| chr17:19648609-19649113 | Common:3; Rare:184; Clinvar (benign):1 | ||||
| chr17:19748257-19748408 | Common:1; Rare:42 | ||||
| chr17:19748470-19748657 | Common:2; Rare:31 | ||||
| chr17:21214144-21214368 | Common:2; Rare:102 | ||||
| chr17:27293953-27294155 | Common:2; Rare:91 | ||||
| chr17:27294545-27294753 | Common:1; Rare:44 | ||||
| chr17:28335359-28335850 | Common:1; Rare:116 | ||||
| chr17:28357400-28357685 | Common:6; Rare:140 | ||||
| chr17:28571497-28571615 | Rare:28 | ||||
| chr17:28598994-28599170 | Common:2; Rare:49 | ||||
| chr17:28645034-28645361 | Common:1; Rare:138 | ||||
| chr17:28661872-28661935 | Rare:32 | ||||
| chr17:28662128-28662327 | Rare:78 |