Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:70523494-70523857 | Common:3; Rare:130; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr16:72093595-72093928 | Rare:79 | ||||
chr16:74296725-74296883 | Rare:61 | ||||
chr16:75433465-75433795 | Common:4; Rare:90 | ||||
chr16:75566242-75566419 | Common:1; Rare:94 | ||||
chr16:75647628-75647867 | Common:4; Rare:120; Clinvar:4 | ||||
chr16:75648071-75648203 | Rare:57 | ||||
chr16:77190680-77191007 | Common:12; Rare:108 | ||||
chr16:77191118-77191224 | Common:1; Rare:49 | ||||
chr16:81006807-81007263 | Common:4; Rare:155 | ||||
chr16:82170180-82170359 | Common:3; Rare:92 | ||||
chr16:84116797-84117067 | Common:3; Rare:108 | ||||
chr16:84504596-84504864 | Common:8; Rare:115 | ||||
chr16:85027611-85027782 | Common:1; Rare:89 | ||||
chr16:85799509-85799760 | Common:2; Rare:76 |