| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:30235693-30235976 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:30291918-30292126 | Rare:75 | ||||
| chr17:30477250-30477449 | Common:1; Rare:58 | ||||
| chr17:30824567-30824859 | Common:3; Rare:115 | ||||
| chr17:30831758-30832004 | Common:1; Rare:63 | ||||
| chr17:30906205-30906371 | Common:1; Rare:46 | ||||
| chr17:31321588-31321770 | Common:3; Rare:29 | ||||
| chr17:32142425-32142702 | Common:7; Rare:117 | ||||
| chr17:32350033-32350198 | Rare:88 | ||||
| chr17:34255086-34255421 | Rare:95 | ||||
| chr17:34961489-34961575 | Common:1; Rare:43 | ||||
| chr17:34980371-34980618 | Common:4; Rare:71 | ||||
| chr17:34981146-34981452 | Common:2; Rare:61 | ||||
| chr17:35147392-35147883 | Common:1; Rare:88 | ||||
| chr17:35242901-35243087 | Rare:62 |