| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4833259-4833560 | Common:1; Rare:76 | ||||
| chr17:4899384-4899460 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:4939916-4940333 | Common:2; Rare:123 | ||||
| chr17:4987640-4987726 | Rare:35 | ||||
| chr17:5078351-5078523 | Common:4; Rare:52 | ||||
| chr17:5191838-5192112 | Common:2; Rare:88 | ||||
| chr17:5419639-5420213 | Common:6; Rare:179 | ||||
| chr17:5486140-5486595 | Common:5; Rare:160 | ||||
| chr17:5486801-5486933 | Common:4; Rare:40 | ||||
| chr17:6640646-6641077 | Common:7; Rare:131 | ||||
| chr17:6651553-6651795 | Common:1; Rare:84 | ||||
| chr17:6831667-6831852 | Rare:31 | ||||
| chr17:7012306-7012686 | Rare:131 | ||||
| chr17:7043013-7043175 | Common:2; Rare:57 | ||||
| chr17:7219726-7219922 | Common:2; Rare:69; Clinvar:3 |