| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50198156-50198504 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50199556-50199935 | Common:7; Rare:128; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50201408-50201697 | Common:2; Rare:83; Clinvar:4; Clinvar (benign):4 | ||||
| chr17:50345911-50346166 | Common:4; Rare:84 | ||||
| chr17:50372942-50373242 | Common:2; Rare:107 | ||||
| chr17:50719469-50719830 | Rare:116 | ||||
| chr17:50866350-50866638 | Common:3; Rare:85 | ||||
| chr17:51166242-51166952 | Common:4; Rare:188 | ||||
| chr17:51260308-51260601 | Common:3; Rare:122 | ||||
| chr17:54968589-54968799 | Common:3; Rare:97 | ||||
| chr17:56833830-56834151 | Common:3; Rare:90 | ||||
| chr17:56914017-56914187 | Rare:46 | ||||
| chr17:57850015-57850266 | Common:1; Rare:78 | ||||
| chr17:57955266-57955411 | Rare:32 | ||||
| chr17:57988093-57988268 | Common:1; Rare:47 |