Variant report

Variant	rs1391393
Chromosome Location	chr4:125950456-125950457
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1303723	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1391395	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2201824	0.85[ASN][1000 genomes]
rs56189956	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72687657	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72687662	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72687666	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72687670	0.87[AMR][1000 genomes];0.88[EUR][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	nsv1001338	chr4:125708756-126103293	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region	3 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	chr4:125949400-125951400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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

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