| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:38925343-38925623 | Common:4; Rare:55 | ||||
| chr17:39608503-39608836 | Rare:51 | ||||
| chr17:41665986-41666128 | Rare:41 | ||||
| chr17:43315777-43315916 | Common:5; Rare:76 | ||||
| chr17:45147488-45147544 | Rare:11 | ||||
| chr17:45149821-45149994 | Common:1; Rare:41 | ||||
| chr17:45172492-45172806 | Common:1; Rare:67 | ||||
| chr17:45585176-45585213 | Rare:3 | ||||
| chr17:45895397-45895448 | Common:1; Rare:9 | ||||
| chr17:45895598-45895781 | Common:2; Rare:48 | ||||
| chr17:47492466-47492505 | Common:1; Rare:17 | ||||
| chr17:49192893-49193095 | Common:2; Rare:49 | ||||
| chr17:49361085-49361373 | Rare:65 | ||||
| chr17:50189694-50189862 | Common:3; Rare:39; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:50189883-50190356 | Common:2; Rare:139; Clinvar:5; Clinvar (benign):5 |