Variant report

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv396936	chr8:129845971-129846002	Weak transcription	n/a	n/a	inside rSNPs	diseases
2	esv1004882	chr8:129845990-129846026	Weak transcription	n/a	n/a	inside rSNPs	diseases
3	esv1333553	chr8:129845990-129846028	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129843800-129863600	Weak transcription	Dnd41	blood
2	chr8:129844800-129847600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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