| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19378115-19378575 | Common:2; Rare:109 | ||||
| chr17:19648581-19649013 | Common:4; Rare:150; Clinvar (benign):1 | ||||
| chr17:19748251-19748692 | Common:3; Rare:107 | ||||
| chr17:19977796-19977967 | Common:1; Rare:59 | ||||
| chr17:21214144-21214361 | Common:2; Rare:99 | ||||
| chr17:27293969-27294149 | Common:2; Rare:81 | ||||
| chr17:27294279-27294380 | Common:1; Rare:31 | ||||
| chr17:28318892-28319259 | Common:3; Rare:130 | ||||
| chr17:28335382-28335841 | Common:1; Rare:110 | ||||
| chr17:28357324-28357679 | Common:11; Rare:161 | ||||
| chr17:28576848-28577054 | Common:2; Rare:55 | ||||
| chr17:28598970-28599131 | Common:1; Rare:56 | ||||
| chr17:28645094-28645230 | Common:1; Rare:55 | ||||
| chr17:28661876-28661945 | Rare:33 | ||||
| chr17:28662106-28662314 | Rare:85 |