Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:89201654-89201997 | Common:4; Rare:116 | ||||
chr16:89217598-89217749 | Common:1; Rare:74 | ||||
chr16:89490532-89490982 | Common:6; Rare:155 | ||||
chr16:89508262-89508592 | Common:3; Rare:167; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr16:89560537-89560962 | Rare:181 | ||||
chr16:89613494-89613699 | Rare:60 | ||||
chr16:89657647-89658098 | Common:3; Rare:236 | ||||
chr16:89686574-89686767 | Common:8; Rare:100 | ||||
chr16:89686913-89687038 | Common:1; Rare:55 | ||||
chr16:89687309-89687359 | Rare:9 | ||||
chr16:89701666-89701839 | Rare:70 | ||||
chr16:89711592-89711901 | Common:3; Rare:112 | ||||
chr16:89816593-89816836 | Common:6; Rare:136; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr16:89828317-89828536 | Rare:92 | ||||
chr16:89910372-89910660 | Common:2; Rare:105 |