| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49414833-49415120 | Common:1; Rare:68 | ||||
| chr17:50055697-50055977 | Common:4; Rare:54 | ||||
| chr17:50186638-50187123 | Common:2; Rare:143; Clinvar:7; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr17:50188740-50188995 | Rare:68; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50373160-50373276 | Common:3; Rare:48 | ||||
| chr17:50719452-50719654 | Rare:79 | ||||
| chr17:51260372-51260587 | Common:3; Rare:100 | ||||
| chr17:54968589-54968792 | Common:3; Rare:95 | ||||
| chr17:56914015-56914180 | Rare:43 | ||||
| chr17:57084980-57085316 | Rare:112 | ||||
| chr17:57849995-57850281 | Common:1; Rare:94 | ||||
| chr17:58007216-58007451 | Common:1; Rare:100 | ||||
| chr17:58352134-58352495 | Common:6; Rare:136 | ||||
| chr17:58692520-58692697 | Common:2; Rare:95; Clinvar:19; Clinvar (benign):20 | ||||
| chr17:59106707-59107059 | Common:2; Rare:116; Clinvar:4; Clinvar (benign):2 |