Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42315864-42315888 | Rare:2 | ||||
chr17:42422520-42422573 | Rare:12 | ||||
chr17:42422613-42422924 | Rare:127; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr17:43315650-43315916 | Common:6; Rare:113 | ||||
chr17:43333313-43333529 | Common:1; Rare:42 | ||||
chr17:43388289-43388411 | Rare:22 | ||||
chr17:44083803-44084095 | Common:1; Rare:72 | ||||
chr17:44096822-44097120 | Common:3; Rare:42 | ||||
chr17:44113779-44113881 | Rare:22 | ||||
chr17:44215634-44215976 | Common:1; Rare:74 | ||||
chr17:45149011-45149607 | Common:4; Rare:197 | ||||
chr17:45150002-45150120 | Rare:21 | ||||
chr17:45247771-45247975 | Common:1; Rare:34 | ||||
chr17:45430923-45431103 | Common:1; Rare:31 | ||||
chr17:45576978-45577102 | Rare:24 |