Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:45060971-45061339 | Common:2; Rare:97 | ||||
chr17:45147964-45148631 | Common:2; Rare:200 | ||||
chr17:45161494-45161926 | Common:1; Rare:114 | ||||
chr17:45317008-45317343 | Common:4; Rare:82 | ||||
chr17:45490708-45490889 | Rare:61 | ||||
chr17:45620232-45620376 | Rare:35 | ||||
chr17:45894208-45894686 | Common:5; Rare:139; Clinvar:5; Clinvar (benign):3 | ||||
chr17:45894852-45894955 | Rare:23 | ||||
chr17:46192711-46192949 | Common:3; Rare:57; Clinvar (benign):4 | ||||
chr17:46193327-46193611 | Common:5; Rare:80 | ||||
chr17:46194026-46194119 | Common:4; Rare:21 | ||||
chr17:46225347-46225488 | Common:2; Rare:37 | ||||
chr17:46579669-46579840 | Rare:12 | ||||
chr17:46833056-46833219 | Common:1; Rare:26 | ||||
chr17:46922831-46923209 | Common:5; Rare:112; Clinvar:3; Clinvar (benign):8 |