| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45161494-45161705 | Rare:55 | ||||
| chr17:45317008-45317343 | Common:4; Rare:82 | ||||
| chr17:45490690-45490793 | Common:1; Rare:40 | ||||
| chr17:45894222-45894610 | Common:4; Rare:119; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:46192556-46192588 | Rare:6 | ||||
| chr17:46192843-46193008 | Common:1; Rare:41 | ||||
| chr17:46193312-46193599 | Common:5; Rare:80 | ||||
| chr17:46225353-46225482 | Common:2; Rare:34 | ||||
| chr17:46833062-46833219 | Common:1; Rare:26 | ||||
| chr17:46922845-46923187 | Common:4; Rare:95; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47188784-47189048 | Common:2; Rare:52 | ||||
| chr17:47189083-47189627 | Common:1; Rare:148 | ||||
| chr17:47253684-47253921 | Common:4; Rare:71; Clinvar (benign):4 | ||||
| chr17:47323841-47323992 | Common:3; Rare:54 | ||||
| chr17:47649614-47650022 | Common:1; Rare:152 |