| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44324782-44324996 | Common:2; Rare:76 | ||||
| chr17:44351150-44351441 | Common:1; Rare:80; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:44708545-44708692 | Rare:33 | ||||
| chr17:44899383-44899449 | Rare:31 | ||||
| chr17:45060933-45061350 | Common:3; Rare:110 | ||||
| chr17:45148265-45148512 | Rare:99 | ||||
| chr17:47649614-47649987 | Common:1; Rare:142 | ||||
| chr17:47831462-47831695 | Rare:76 | ||||
| chr17:47895770-47896274 | Common:2; Rare:148 | ||||
| chr17:47941411-47941625 | Rare:44; Clinvar:1 | ||||
| chr17:48048048-48048372 | Rare:86 | ||||
| chr17:48048599-48048813 | Common:4; Rare:31 | ||||
| chr17:48544446-48544618 | Common:1; Rare:63 | ||||
| chr17:49788582-49788707 | Rare:36 | ||||
| chr17:50055915-50056128 | Common:4; Rare:53 |