Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:740944-741145 | Rare:69 | ||||
chr16:1493247-1493587 | Common:4; Rare:103 | ||||
chr16:1612032-1612362 | Common:2; Rare:111; Clinvar:1 | ||||
chr16:1706042-1706281 | Common:2; Rare:71 | ||||
chr16:1771502-1771863 | Common:3; Rare:141 | ||||
chr16:1782510-1783009 | Common:4; Rare:165 | ||||
chr16:1827157-1827232 | Common:1; Rare:33 | ||||
chr16:1943189-1943505 | Common:1; Rare:94 | ||||
chr16:1964814-1964998 | Common:6; Rare:82 | ||||
chr16:1971803-1972110 | Common:3; Rare:91 | ||||
chr16:1975041-1975216 | Common:2; Rare:77 | ||||
chr16:2009691-2009891 | Common:15; Rare:83 | ||||
chr16:2033125-2033272 | Rare:32 | ||||
chr16:2047793-2048058 | Rare:130; Clinvar:2; Clinvar (benign):5 | ||||
chr16:2223344-2223666 | Rare:130 |