| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39637497-39637624 | Common:2; Rare:28 | ||||
| chr17:39687425-39687464 | Common:1; Rare:6 | ||||
| chr17:39687743-39688316 | Rare:182; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:39688591-39688686 | Rare:23 | ||||
| chr17:39699816-39700239 | Rare:102 | ||||
| chr17:39700381-39700503 | Common:1; Rare:23 | ||||
| chr17:39700701-39700786 | Rare:16 | ||||
| chr17:39730055-39730135 | Common:1; Rare:16 | ||||
| chr17:39730211-39730636 | Common:1; Rare:143 | ||||
| chr17:39737785-39737974 | Rare:25 | ||||
| chr17:39738141-39738369 | Common:1; Rare:52 | ||||
| chr17:39738605-39738819 | Rare:36 | ||||
| chr17:39739284-39739540 | Rare:46 | ||||
| chr17:39739638-39739846 | Common:1; Rare:39 | ||||
| chr17:39740051-39740168 | Rare:22 |