| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17591589-17591926 | Common:2; Rare:96 | ||||
| chr17:18039155-18039410 | Common:3; Rare:64; Clinvar (benign):1 | ||||
| chr17:18183023-18183111 | Rare:30 | ||||
| chr17:18184032-18184395 | Common:1; Rare:166 | ||||
| chr17:18254584-18254824 | Rare:80 | ||||
| chr17:18314921-18315332 | Common:1; Rare:117 | ||||
| chr17:18781076-18781301 | Common:5; Rare:62 | ||||
| chr17:18856195-18856378 | Common:1; Rare:32 | ||||
| chr17:19377613-19377773 | Common:2; Rare:41 | ||||
| chr17:19377905-19378033 | Common:1; Rare:30 | ||||
| chr17:19378153-19378537 | Common:2; Rare:95 | ||||
| chr17:19648627-19648810 | Common:2; Rare:61 | ||||
| chr17:19977804-19977936 | Common:1; Rare:42 | ||||
| chr17:21042234-21042429 | Common:1; Rare:73 | ||||
| chr17:21214140-21214322 | Common:2; Rare:75 |