| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:18856102-18856415 | Common:1; Rare:63 | ||||
| chr17:18857869-18858349 | Common:7; Rare:108 | ||||
| chr17:18858358-18858449 | Common:1; Rare:18 | ||||
| chr17:19004121-19004375 | Common:1; Rare:56 | ||||
| chr17:19004662-19004954 | Common:2; Rare:70 | ||||
| chr17:19237306-19237370 | Common:1; Rare:25 | ||||
| chr17:19362314-19362406 | Rare:8 | ||||
| chr17:19362606-19362852 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:19362916-19363127 | Common:2; Rare:49 | ||||
| chr17:19377607-19378223 | Common:5; Rare:145 | ||||
| chr17:19378230-19378586 | Common:2; Rare:80 | ||||
| chr17:19647994-19648196 | Common:1; Rare:47 | ||||
| chr17:19648235-19648282 | Rare:15 | ||||
| chr17:19648346-19649172 | Common:5; Rare:268; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:19672021-19672259 | Rare:45 |