Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:31471931-31472181 | Rare:55 | ||||
chr16:31508369-31508424 | Rare:26 | ||||
chr16:46973632-46973772 | Rare:67 | ||||
chr16:47461046-47461362 | Common:2; Rare:113; Clinvar (benign):2 | ||||
chr16:53703828-53704167 | Rare:96; Clinvar:3 | ||||
chr16:56451309-56451600 | Common:1; Rare:91 | ||||
chr16:56608323-56608725 | Common:4; Rare:118 | ||||
chr16:56931909-56932147 | Common:2; Rare:112 | ||||
chr16:57185961-57186335 | Common:1; Rare:106 | ||||
chr16:57447371-57447504 | Common:2; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
chr16:58001210-58001436 | Common:1; Rare:47 | ||||
chr16:66552476-66552636 | Rare:69 | ||||
chr16:66934365-66934506 | Rare:50 | ||||
chr16:67226916-67227187 | Rare:109 | ||||
chr16:67846792-67846976 | Common:1; Rare:51 |