| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76578490-76578710 | Common:1; Rare:43 | ||||
| chr17:76629390-76629870 | Common:5; Rare:134 | ||||
| chr17:76642908-76643206 | Common:3; Rare:57 | ||||
| chr17:76643579-76643856 | Common:7; Rare:263 | ||||
| chr17:76643821-76644221 | Common:1; Rare:68 | ||||
| chr17:76709132-76709667 | Common:2; Rare:236 | ||||
| chr17:76710230-76711170 | Common:13; Rare:343 | ||||
| chr17:76725710-76726238 | Common:3; Rare:501 | ||||
| chr17:76726367-76726994 | Common:34; Rare:1173 | ||||
| chr17:76727000-76727400 | Common:6; Rare:210 | ||||
| chr17:76732846-76733246 | Common:2; Rare:233; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr17:76734979-76735580 | Rare:215 | ||||
| chr17:76736036-76737191 | Common:7; Rare:1251; Clinvar:1 | ||||
| chr17:76737131-76737760 | Common:32; Rare:1203 | ||||
| chr17:76737760-76738142 | Common:28; Rare:631 |