Variant report

Variant	rs2030741
Chromosome Location	chr7:108757830-108757831
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10225252	0.97[ASN][1000 genomes]
rs10227370	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10272130	0.97[ASN][1000 genomes]
rs10275557	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11770410	0.94[ASN][1000 genomes]
rs1404584	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1404585	0.97[ASN][1000 genomes]
rs1404586	0.90[EUR][1000 genomes]
rs1525023	0.97[ASN][1000 genomes]
rs1525037	0.84[EUR][1000 genomes]
rs1581541	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2030738	0.97[ASN][1000 genomes]
rs2030739	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4143238	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4595060	0.88[EUR][1000 genomes]
rs6948286	0.92[ASN][1000 genomes]
rs6970149	0.97[ASN][1000 genomes]
rs7782995	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]

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	nsv831091	chr7:108756218-108923644	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 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	chr7:108752600-108766800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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