| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44215928-44216242 | Common:3; Rare:75 | ||||
| chr17:44556670-44556779 | Rare:24 | ||||
| chr17:45247754-45247977 | Common:1; Rare:39 | ||||
| chr17:45248295-45248392 | Common:2; Rare:15 | ||||
| chr17:45584755-45585103 | Common:2; Rare:49 | ||||
| chr17:45585176-45585213 | Rare:3 | ||||
| chr17:45586248-45586497 | Common:5; Rare:26 | ||||
| chr17:47100234-47100431 | Common:1; Rare:55 | ||||
| chr17:47437027-47437252 | Common:1; Rare:33 | ||||
| chr17:47492436-47492498 | Common:2; Rare:29 | ||||
| chr17:48050476-48050650 | Common:1; Rare:36 | ||||
| chr17:49192912-49193152 | Common:2; Rare:56 | ||||
| chr17:50055205-50055274 | Common:1; Rare:15 | ||||
| chr17:50189876-50190109 | Common:1; Rare:69; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:50660739-50661037 | Common:1; Rare:70 |