Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:50742704-50742815 | Rare:20 | ||||
chr16:53054852-53055068 | Common:1; Rare:49 | ||||
chr16:53703821-53704185 | Rare:106; Clinvar:4; Clinvar (benign):1 | ||||
chr16:55833002-55833407 | Common:12; Rare:129 | ||||
chr16:56191077-56191385 | Common:5; Rare:107 | ||||
chr16:56451303-56451619 | Common:1; Rare:106 | ||||
chr16:56519975-56520131 | Common:4; Rare:60; Clinvar:6; Clinvar (benign):5 | ||||
chr16:56608171-56608428 | Common:1; Rare:58 | ||||
chr16:56608435-56608756 | Common:3; Rare:96 | ||||
chr16:56625494-56625879 | Common:1; Rare:112 | ||||
chr16:56632461-56632740 | Common:2; Rare:89 | ||||
chr16:56638514-56638731 | Common:1; Rare:88 | ||||
chr16:56657450-56657837 | Common:1; Rare:85 | ||||
chr16:56657850-56658045 | Common:2; Rare:56 | ||||
chr16:56682127-56682578 | Common:8; Rare:134 |