| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1684771-1685070 | Common:2; Rare:103; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1829766-1830038 | Common:6; Rare:116 | ||||
| chr17:2303504-2303558 | Rare:19 | ||||
| chr17:2303709-2303987 | Common:2; Rare:106 | ||||
| chr17:2336430-2336550 | Rare:46 | ||||
| chr17:2511812-2511926 | Common:2; Rare:31 | ||||
| chr17:2593460-2593697 | Common:3; Rare:91; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:2593857-2593999 | Common:1; Rare:38; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:3636241-3636757 | Common:8; Rare:141; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:3668532-3668861 | Common:3; Rare:136 | ||||
| chr17:3723764-3723922 | Common:1; Rare:87 | ||||
| chr17:4143028-4143244 | Rare:69 | ||||
| chr17:4143597-4143763 | Common:4; Rare:98 | ||||
| chr17:4263943-4264096 | Rare:61 | ||||
| chr17:4366632-4366806 | Common:1; Rare:69 |