| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8164584-8164984 | Common:2; Rare:107 | ||||
| chr17:8173444-8173903 | Common:16; Rare:331; Clinvar:3; Clinvar (pathogenic):3 | ||||
| chr17:8186822-8186957 | Common:1; Rare:95 | ||||
| chr17:8187442-8187682 | Common:6; Rare:130 | ||||
| chr17:8192231-8192408 | Common:2; Rare:27 | ||||
| chr17:8200191-8200341 | Rare:34 | ||||
| chr17:8221448-8221621 | Common:2; Rare:118 | ||||
| chr17:8222240-8222348 | Common:1; Rare:96 | ||||
| chr17:8223022-8223192 | Rare:49 | ||||
| chr17:8223460-8223586 | Common:2; Rare:25 | ||||
| chr17:8226500-8226880 | Common:3; Rare:187; Clinvar:15; Clinvar (benign):1 | ||||
| chr17:8629302-8629433 | Rare:30 | ||||
| chr17:8629503-8629802 | Common:1; Rare:68 | ||||
| chr17:8631294-8631561 | Common:1; Rare:86 | ||||
| chr17:8631828-8632525 | Common:5; Rare:158 |