| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50198167-50198503 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50199416-50199963 | Common:8; Rare:173; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:50345926-50346136 | Common:4; Rare:69 | ||||
| chr17:50373160-50373261 | Common:3; Rare:44 | ||||
| chr17:50719504-50719704 | Rare:84 | ||||
| chr17:50866351-50866783 | Common:3; Rare:119 | ||||
| chr17:51166372-51166863 | Common:4; Rare:131 | ||||
| chr17:51259988-51260142 | Rare:50 | ||||
| chr17:51260362-51260581 | Common:3; Rare:99 | ||||
| chr17:54968558-54968799 | Common:3; Rare:106 | ||||
| chr17:56914029-56914175 | Rare:35 | ||||
| chr17:57084980-57085335 | Rare:119 | ||||
| chr17:57256849-57257050 | Rare:64 | ||||
| chr17:57850006-57850274 | Common:1; Rare:86 | ||||
| chr17:58007155-58007372 | Common:1; Rare:106 |