Variant report

Variant	rs374058610
Chromosome Location	chrY:5999271-5999272
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	esv2758598	chrY:5955799-6326452	Enhancers Weak transcription Active TSS	TF binding region CpG island lncRNA	24 gene(s)	inside rSNPs	diseases
2	esv2758903	chrY:5955799-6326452	Weak transcription Enhancers Active TSS	TF binding region CpG island lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv510872	chrY:5975458-6038342	Active TSS Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrY:5999000-5999400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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