Variant report

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1273296	chr6:46077847-46077848	Weak transcription	n/a	n/a	inside rSNPs	diseases

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Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:46063000-46080800	Weak transcription	Primary T cells from cord blood	blood
2	chr6:46071600-46086800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr6:46075800-46081200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr6:46075800-46081400	Weak transcription	Fetal Intestine Small	intestine

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