| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39715290-39715535 | Rare:70; Clinvar:3 | ||||
| chr17:39724837-39725199 | Rare:95; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr17:39727539-39727733 | Rare:54; Clinvar:2 | ||||
| chr17:40088996-40089267 | Common:5; Rare:61 | ||||
| chr17:40099288-40099466 | Common:2; Rare:47 | ||||
| chr17:40179037-40179273 | Common:1; Rare:56 | ||||
| chr17:41549847-41550066 | Common:4; Rare:31 | ||||
| chr17:41554493-41554665 | Common:1; Rare:29 | ||||
| chr17:41555062-41555131 | Rare:6 | ||||
| chr17:41648548-41648663 | Rare:23 | ||||
| chr17:41651639-41651831 | Rare:42 | ||||
| chr17:41757420-41757647 | Common:2; Rare:81; Clinvar:8; Clinvar (benign):12 | ||||
| chr17:41769052-41769419 | Common:2; Rare:109; Clinvar:15; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr17:41769668-41769686 | Common:1; Rare:3; Clinvar (benign):1 | ||||
| chr17:41973297-41973625 | Common:2; Rare:87 |