| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7583739-7583865 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7687457-7687654 | Rare:41; Clinvar:1 | ||||
| chr17:7857113-7857357 | Common:1; Rare:129 | ||||
| chr17:7857383-7857758 | Common:3; Rare:124 | ||||
| chr17:7885194-7885350 | Rare:51 | ||||
| chr17:7931890-7932267 | Common:5; Rare:102 | ||||
| chr17:8162937-8163108 | Rare:58 | ||||
| chr17:8176306-8176441 | Rare:46 | ||||
| chr17:8210555-8210712 | Common:2; Rare:30 | ||||
| chr17:8248042-8248136 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8435715-8436006 | Common:4; Rare:116 | ||||
| chr17:10697481-10697660 | Common:4; Rare:80; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:13601906-13602160 | Common:3; Rare:80 | ||||
| chr17:14069384-14069571 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:15999586-16000028 | Common:3; Rare:187; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 |