| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50194571-50194830 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:50195232-50195667 | Rare:117; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:50196197-50196318 | Common:1; Rare:41; Clinvar:1 | ||||
| chr17:50198160-50198504 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50373160-50373242 | Common:2; Rare:35 | ||||
| chr17:50707621-50707840 | Common:4; Rare:71 | ||||
| chr17:50719452-50719661 | Rare:83 | ||||
| chr17:50866351-50866644 | Common:3; Rare:86 | ||||
| chr17:51260361-51260587 | Common:3; Rare:102 | ||||
| chr17:54968631-54968799 | Common:3; Rare:79 | ||||
| chr17:57084980-57085346 | Rare:121 | ||||
| chr17:57850013-57850274 | Common:1; Rare:80 | ||||
| chr17:58007189-58007380 | Common:1; Rare:85 | ||||
| chr17:58219226-58219284 | Common:1; Rare:27; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:58692501-58692668 | Common:2; Rare:92; Clinvar:10; Clinvar (benign):20 |