| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4899324-4899489 | Common:1; Rare:111; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr17:4939916-4940136 | Common:2; Rare:74 | ||||
| chr17:4948144-4948384 | Rare:74 | ||||
| chr17:4948954-4949073 | Common:1; Rare:39 | ||||
| chr17:4967767-4967909 | Rare:60 | ||||
| chr17:5191838-5192123 | Common:2; Rare:91 | ||||
| chr17:5419625-5420225 | Common:6; Rare:194 | ||||
| chr17:5486157-5486581 | Common:5; Rare:143 | ||||
| chr17:5486776-5486920 | Common:4; Rare:46 | ||||
| chr17:6640646-6641084 | Common:7; Rare:134 | ||||
| chr17:6651500-6651767 | Common:1; Rare:92 | ||||
| chr17:7012315-7012692 | Rare:130 | ||||
| chr17:7221317-7221589 | Common:9; Rare:81; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr17:7234319-7234634 | Common:2; Rare:137 | ||||
| chr17:7241602-7241896 | Common:1; Rare:63 |