Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:3305279-3305514 | Common:3; Rare:75 | ||||
chr16:3400967-3401220 | Common:6; Rare:92 | ||||
chr16:4734262-4734537 | Rare:83 | ||||
chr16:5097793-5098041 | Common:4; Rare:71 | ||||
chr16:8797618-8797883 | Rare:104; Clinvar:2; Clinvar (benign):2 | ||||
chr16:11345282-11345464 | Common:1; Rare:59 | ||||
chr16:11976641-11976755 | Rare:39 | ||||
chr16:20806441-20806527 | Rare:35 | ||||
chr16:21599364-21599660 | Common:4; Rare:104 | ||||
chr16:23641279-23641524 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
chr16:24729503-24729753 | Common:6; Rare:107 | ||||
chr16:25111521-25111758 | Common:2; Rare:59 | ||||
chr16:27268717-27268844 | Common:1; Rare:39 | ||||
chr16:27549892-27550158 | Common:2; Rare:93 | ||||
chr16:28823964-28824122 | Common:1; Rare:45 |