| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44066523-44067051 | Common:3; Rare:326 | ||||
| chr17:44070510-44070979 | Common:9; Rare:376; Clinvar:12; Clinvar (benign):6 | ||||
| chr17:44071090-44071934 | Common:3; Rare:324; Clinvar:2; Clinvar (pathogenic):4 | ||||
| chr17:44111169-44111470 | Rare:221 | ||||
| chr17:44123523-44123912 | Common:8; Rare:234 | ||||
| chr17:44123930-44124290 | Common:2; Rare:140 | ||||
| chr17:44141756-44142112 | Common:3; Rare:235 | ||||
| chr17:44186524-44187066 | Common:6; Rare:482 | ||||
| chr17:44187080-44187314 | Common:2; Rare:139 | ||||
| chr17:44198220-44198914 | Common:7; Rare:409 | ||||
| chr17:44199306-44199568 | Common:4; Rare:197 | ||||
| chr17:44199665-44199810 | Rare:55 | ||||
| chr17:44199827-44200568 | Common:8; Rare:597 | ||||
| chr17:44212513-44214543 | Common:12; Rare:750 | ||||
| chr17:44218194-44218482 | Common:1; Rare:75 |