| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8176291-8176455 | Rare:59 | ||||
| chr17:8248042-8248122 | Common:2; Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249203-8249317 | Common:1; Rare:32 | ||||
| chr17:8435715-8436042 | Common:4; Rare:123 | ||||
| chr17:8867638-8867776 | Common:1; Rare:23 | ||||
| chr17:8965674-8965823 | Common:1; Rare:43 | ||||
| chr17:10421921-10422222 | Common:2; Rare:57 | ||||
| chr17:10630398-10630745 | Common:2; Rare:95; Clinvar:2 | ||||
| chr17:10697503-10697654 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:10729553-10729816 | Common:3; Rare:101 | ||||
| chr17:11997444-11997586 | Rare:49 | ||||
| chr17:14069395-14069580 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:15260723-15260927 | Rare:79; Clinvar (benign):4 | ||||
| chr17:15563436-15563694 | Rare:95 | ||||
| chr17:15999578-16000028 | Common:3; Rare:189; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 |