| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42833367-42833588 | Common:1; Rare:70 | ||||
| chr17:42851052-42851346 | Rare:73 | ||||
| chr17:42851438-42851536 | Rare:33 | ||||
| chr17:42852303-42852460 | Common:2; Rare:46 | ||||
| chr17:42964405-42964528 | Rare:60 | ||||
| chr17:42980408-42980576 | Common:1; Rare:55 | ||||
| chr17:42998118-42998485 | Common:3; Rare:98 | ||||
| chr17:43125331-43125685 | Rare:86; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43170223-43170720 | Common:3; Rare:103 | ||||
| chr17:43171024-43171245 | Rare:68 | ||||
| chr17:43211778-43211903 | Common:1; Rare:26 | ||||
| chr17:43778812-43779041 | Rare:48 | ||||
| chr17:44005894-44006026 | Rare:43 | ||||
| chr17:44066594-44066836 | Common:1; Rare:90 | ||||
| chr17:44070612-44070918 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):2 |