| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:54968509-54968980 | Common:29; Rare:727 | ||||
| chr17:54969061-54969519 | Common:13; Rare:181 | ||||
| chr17:55264650-55265090 | Common:2; Rare:160 | ||||
| chr17:55420924-55421815 | Common:6; Rare:233 | ||||
| chr17:55421832-55422273 | Common:14; Rare:596 | ||||
| chr17:55722642-55723118 | Common:4; Rare:147 | ||||
| chr17:55731307-55731769 | Common:4; Rare:133 | ||||
| chr17:55731766-55732030 | Common:5; Rare:98 | ||||
| chr17:55732050-55732430 | Common:2; Rare:104 | ||||
| chr17:55750732-55751232 | Common:12; Rare:410 | ||||
| chr17:55751163-55751830 | Common:17; Rare:415 | ||||
| chr17:56833281-56833770 | Common:7; Rare:280 | ||||
| chr17:56833820-56834222 | Common:20; Rare:733 | ||||
| chr17:56834554-56834956 | Common:3; Rare:182; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:56835108-56835508 | Common:1; Rare:127 |