Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:20900931-20901262 | Common:1; Rare:80 | ||||
chr16:21599361-21599784 | Common:4; Rare:153 | ||||
chr16:21952975-21953456 | Common:1; Rare:122; Clinvar (benign):3 | ||||
chr16:22007562-22007620 | Common:1; Rare:8 | ||||
chr16:22008371-22008462 | Rare:40 | ||||
chr16:22436939-22437106 | Rare:62 | ||||
chr16:22437110-22437320 | Rare:70 | ||||
chr16:22437348-22437443 | Rare:31 | ||||
chr16:22437518-22437613 | Common:2; Rare:29 | ||||
chr16:23453114-23453262 | Rare:47 | ||||
chr16:23557294-23557483 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):3 | ||||
chr16:23641238-23641545 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):3 | ||||
chr16:23835862-23836182 | Common:3; Rare:101 | ||||
chr16:24539424-24539637 | Common:1; Rare:87 | ||||
chr16:24729597-24729844 | Common:7; Rare:104 |