Variant report

Variant	rs73817048
Chromosome Location	chr4:54613126-54613127
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs17083362	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs3762880	0.92[ASN][1000 genomes]
rs3915416	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs56982325	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs60077509	0.82[ASN][1000 genomes]
rs6554124	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6811080	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs714146	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs73817047	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7686371	0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7699271	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7699804	0.83[AMR][1000 genomes];0.82[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	nsv879015	chr4:54596466-54665559	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:54612000-54616000	Enhancers	Primary B cells from peripheral blood	blood
2	chr4:54612800-54613600	Enhancers	GM12878-XiMat	blood
3	chr4:54612800-54615000	Enhancers	Primary B cells from cord blood	blood

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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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