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	esv1009136	chr1:220607563-220613446	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220605400-220609200	Weak transcription	Fetal Heart	heart
2	chr1:220606600-220607800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:220606800-220614200	Weak transcription	Fetal Muscle Leg	muscle

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