| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:30116451-30116939 | Common:4; Rare:213 | ||||
| chr17:30116940-30117142 | Rare:53 | ||||
| chr17:30291876-30292228 | Common:2; Rare:175 | ||||
| chr17:30378742-30379022 | Common:2; Rare:212 | ||||
| chr17:30477213-30477490 | Common:2; Rare:173 | ||||
| chr17:30477860-30478230 | Common:3; Rare:98 | ||||
| chr17:30824589-30824992 | Common:10; Rare:351 | ||||
| chr17:30831770-30832063 | Common:1; Rare:171 | ||||
| chr17:30906181-30906475 | Common:3; Rare:177 | ||||
| chr17:30906410-30906610 | Rare:28 | ||||
| chr17:30921753-30921977 | Common:1; Rare:49 | ||||
| chr17:30970417-30970561 | Common:1; Rare:71 | ||||
| chr17:30970828-30971203 | Common:8; Rare:265 | ||||
| chr17:30971259-30971485 | Common:8; Rare:176; Clinvar (benign):3 | ||||
| chr17:31094652-31095032 | Common:6; Rare:215; Clinvar:3 |