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	esv3449168	chr11:60084417-60085198	Weak transcription Flanking Active TSS Enhancers	lncRNA	1 gene(s)	inside rSNPs	n/a

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Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:60083800-60086200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr11:60084400-60086400	Weak transcription	Placenta	Placenta
3	chr11:60085000-60085800	Weak transcription	GM12878-XiMat	blood

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