| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:18856178-18856408 | Common:1; Rare:43 | ||||
| chr17:19004722-19004916 | Common:2; Rare:56 | ||||
| chr17:19362546-19362773 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:19377622-19377856 | Common:2; Rare:60 | ||||
| chr17:19377880-19378035 | Common:1; Rare:39 | ||||
| chr17:19378125-19378608 | Common:2; Rare:111 | ||||
| chr17:19533585-19534066 | Common:4; Rare:130 | ||||
| chr17:19555102-19555294 | Common:1; Rare:46 | ||||
| chr17:19572620-19572825 | Rare:46 | ||||
| chr17:19647935-19648196 | Common:1; Rare:56 | ||||
| chr17:19648583-19649144 | Common:4; Rare:206; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:19977779-19977974 | Common:1; Rare:67 | ||||
| chr17:20009243-20009401 | Common:3; Rare:47 | ||||
| chr17:21011150-21011440 | Common:2; Rare:68 | ||||
| chr17:21214118-21214361 | Common:2; Rare:114 |