| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39199908-39200460 | Common:3; Rare:184 | ||||
| chr17:39200542-39200594 | Common:1; Rare:13 | ||||
| chr17:39401563-39401830 | Common:1; Rare:73 | ||||
| chr17:39402512-39402718 | Rare:60 | ||||
| chr17:39451153-39451481 | Common:5; Rare:115 | ||||
| chr17:39461321-39461726 | Common:1; Rare:101 | ||||
| chr17:39461781-39462213 | Common:3; Rare:124 | ||||
| chr17:39636966-39637412 | Common:6; Rare:152 | ||||
| chr17:39687720-39687953 | Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:39688004-39688224 | Rare:64 | ||||
| chr17:39730211-39730358 | Rare:49 | ||||
| chr17:39730400-39730675 | Common:1; Rare:88 | ||||
| chr17:39777668-39777740 | Rare:17 | ||||
| chr17:39778092-39778143 | Common:1; Rare:11 | ||||
| chr17:39778201-39778231 | Rare:2 |