| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31086215-31086487 | Common:1; Rare:88 | ||||
| chr16:56617400-56617507 | Common:1; Rare:21 | ||||
| chr16:67390247-67390586 | Common:1; Rare:107 | ||||
| chr16:72664938-72665145 | Common:1; Rare:62 | ||||
| chr16:74368124-74368386 | Common:1; Rare:72 | ||||
| chr16:88896876-88897043 | Common:4; Rare:49 | ||||
| chr17:5121219-5121373 | Common:2; Rare:25 | ||||
| chr17:7905872-7906207 | Common:3; Rare:93 | ||||
| chr17:10392624-10393005 | Common:1; Rare:111; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:10399517-10399922 | Common:1; Rare:95; Clinvar (benign):1 | ||||
| chr17:10415111-10415350 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr17:10415470-10415712 | Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:10418643-10418936 | Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:10623745-10624067 | Common:1; Rare:53 | ||||
| chr17:10635364-10635861 | Common:5; Rare:138; Clinvar:4; Clinvar (benign):3 |