| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47099701-47099866 | Rare:38 | ||||
| chr17:47100186-47100541 | Common:3; Rare:95 | ||||
| chr17:47204975-47205277 | Common:2; Rare:43 | ||||
| chr17:47205599-47205807 | Common:2; Rare:32 | ||||
| chr17:47279165-47279412 | Common:2; Rare:38 | ||||
| chr17:47286342-47286419 | Rare:21; Clinvar (pathogenic):3 | ||||
| chr17:47286768-47286858 | Rare:15 | ||||
| chr17:47324679-47324707 | Rare:4 | ||||
| chr17:47324945-47324959 | Rare:1 | ||||
| chr17:47324970-47324995 | Rare:5 | ||||
| chr17:47492415-47492767 | Common:3; Rare:118 | ||||
| chr17:47532120-47532243 | Common:1; Rare:34 | ||||
| chr17:47734537-47734683 | Common:16; Rare:48 | ||||
| chr17:47734837-47735037 | Rare:37 | ||||
| chr17:47735543-47735779 | Rare:34 |