| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50195208-50195672 | Rare:125; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:50196154-50196376 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:50197872-50198207 | Common:5; Rare:90; Clinvar (benign):9 | ||||
| chr17:50199416-50199961 | Common:8; Rare:173; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:50199992-50200268 | Rare:85 | ||||
| chr17:50373174-50373246 | Common:2; Rare:27 | ||||
| chr17:50719452-50719661 | Rare:83 | ||||
| chr17:50866355-50866560 | Common:2; Rare:62 | ||||
| chr17:51260177-51260581 | Common:3; Rare:149 | ||||
| chr17:54968638-54968792 | Common:3; Rare:72 | ||||
| chr17:57850006-57850274 | Common:1; Rare:86 | ||||
| chr17:58007223-58007384 | Common:1; Rare:71 | ||||
| chr17:59106707-59106999 | Common:2; Rare:98; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59619541-59619953 | Common:3; Rare:150 | ||||
| chr17:59707403-59707705 | Common:3; Rare:83; Clinvar (benign):2 |