Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:20900889-20901096 | Common:2; Rare:46 | ||||
chr16:21652602-21652744 | Rare:32 | ||||
chr16:21953024-21953413 | Common:1; Rare:98; Clinvar (benign):3 | ||||
chr16:22092267-22092575 | Rare:50 | ||||
chr16:22436942-22437121 | Rare:65 | ||||
chr16:22437173-22437468 | Rare:93 | ||||
chr16:22437505-22437695 | Common:2; Rare:49 | ||||
chr16:23453154-23453268 | Rare:35 | ||||
chr16:23557343-23557503 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr16:23641219-23641530 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):3 | ||||
chr16:24539351-24539626 | Common:1; Rare:95 | ||||
chr16:24540303-24540462 | Rare:42 | ||||
chr16:24729604-24729745 | Common:6; Rare:74 | ||||
chr16:25015291-25015457 | Common:2; Rare:61 | ||||
chr16:25111521-25111812 | Common:2; Rare:85 |