| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:73291444-73291772 | Common:2; Rare:68 | ||||
| chr17:73293074-73293842 | Common:4; Rare:167 | ||||
| chr17:73305145-73305260 | Common:2; Rare:23 | ||||
| chr17:73308293-73308780 | Common:2; Rare:115 | ||||
| chr17:73340287-73340424 | Rare:20 | ||||
| chr17:73360098-73360291 | Rare:32 | ||||
| chr17:73546901-73547401 | Rare:174 | ||||
| chr17:73760401-73760901 | Common:14; Rare:203 | ||||
| chr17:73956701-73956869 | Common:1; Rare:29 | ||||
| chr17:74042940-74043065 | Common:1; Rare:20 | ||||
| chr17:74199744-74199877 | Common:1; Rare:34 | ||||
| chr17:74296718-74296849 | Rare:21 | ||||
| chr17:74301160-74301490 | Rare:70; Clinvar (benign):1 | ||||
| chr17:74354136-74354295 | Common:5; Rare:65 | ||||
| chr17:74368260-74368590 | Common:2; Rare:70 |