| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39401614-39401813 | Common:1; Rare:55 | ||||
| chr17:39451036-39451406 | Common:3; Rare:116 | ||||
| chr17:39461321-39461558 | Common:1; Rare:68 | ||||
| chr17:39637018-39637176 | Common:2; Rare:48 | ||||
| chr17:39687880-39688103 | Rare:85; Clinvar (pathogenic):1 | ||||
| chr17:39926879-39927073 | Common:1; Rare:37 | ||||
| chr17:39927200-39927325 | Common:1; Rare:21 | ||||
| chr17:39927469-39927732 | Common:2; Rare:75 | ||||
| chr17:39980988-39981195 | Common:1; Rare:70 | ||||
| chr17:40026669-40027023 | Common:1; Rare:96 | ||||
| chr17:40121821-40122041 | Common:2; Rare:80 | ||||
| chr17:40140150-40140568 | Common:5; Rare:195 | ||||
| chr17:40167531-40167942 | Common:1; Rare:89 | ||||
| chr17:40219347-40219441 | Common:2; Rare:46 | ||||
| chr17:40318079-40318319 | Common:1; Rare:53 |