Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:48395112-48395327 | Common:2; Rare:41 | ||||
chr18:48407582-48407891 | Common:1; Rare:48 | ||||
chr18:49563994-49564033 | Rare:10 | ||||
chr18:49564313-49564435 | Common:1; Rare:16 | ||||
chr18:50195671-50195994 | Common:2; Rare:71 | ||||
chr18:50649854-50650107 | Rare:34 | ||||
chr18:55234649-55234952 | Common:2; Rare:58; Clinvar (benign):2 | ||||
chr18:57630208-57630401 | Common:1; Rare:51 | ||||
chr18:57701047-57701144 | Rare:25; Clinvar:2; Clinvar (benign):1 | ||||
chr18:57802020-57802113 | Common:1; Rare:28 | ||||
chr18:59408915-59408983 | |||||
chr18:61652047-61652361 | Common:6; Rare:56 | ||||
chr18:61892981-61893169 | Rare:44 | ||||
chr18:63266791-63267059 | Common:1; Rare:41 | ||||
chr18:63268205-63268220 | Rare:2 |