Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43170960-43171227 | Rare:88 | ||||
chr17:44070618-44070914 | Common:3; Rare:100; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44186705-44187038 | Rare:102 | ||||
chr17:44899375-44899466 | Rare:39 | ||||
chr17:45060971-45061339 | Common:2; Rare:97 | ||||
chr17:47189244-47189579 | Rare:83 | ||||
chr17:47831503-47831658 | Rare:42 | ||||
chr17:48048574-48048842 | Common:4; Rare:52 | ||||
chr17:48055800-48056015 | Rare:33 | ||||
chr17:48544531-48544699 | Rare:84 | ||||
chr17:49210572-49210712 | Rare:19 | ||||
chr17:49788581-49788697 | Rare:31 | ||||
chr17:50195232-50195457 | Rare:67; Clinvar:1; Clinvar (benign):3 | ||||
chr17:51166703-51166954 | Rare:77 | ||||
chr17:54968644-54968727 | Common:3; Rare:49 |