Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:84631270-84631477 | Common:4; Rare:59 | ||||
chr15:89122507-89122815 | Common:3; Rare:55 | ||||
chr16:528826-529178 | Common:2; Rare:92 | ||||
chr16:1204685-1205185 | Common:16; Rare:145; Clinvar:5; Clinvar (benign):1 | ||||
chr16:1206800-1207101 | Common:3; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
chr16:1916546-1916874 | Common:1; Rare:58 | ||||
chr16:1917517-1917642 | Common:2; Rare:24 | ||||
chr16:2673369-2673683 | Common:9; Rare:107 | ||||
chr16:10451974-10452229 | Common:2; Rare:57 | ||||
chr16:21501660-21501784 | Rare:17 | ||||
chr16:21629740-21629832 | Rare:26 | ||||
chr16:23755640-23755926 | Common:1; Rare:95 | ||||
chr16:55330646-55330904 | Common:1; Rare:47 | ||||
chr16:67429586-67429801 | Common:1; Rare:34 | ||||
chr16:74305021-74305619 | Rare:165 |