Variant report

Variant	rs73873757
Chromosome Location	chr3:156701639-156701640
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs13319332	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16827128	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73873759	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73873778	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73873780	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7623552	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7643607	1.00[AMR][1000 genomes]
rs9819460	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9825405	1.00[AMR][1000 genomes]
rs9827477	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9840315	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9864185	1.00[AMR][1000 genomes]
rs9867779	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829765	chr3:156568263-156718496	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3349885	chr3:156685409-156878910	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:156698200-156702200	Weak transcription	Primary B cells from cord blood	blood
2	chr3:156698400-156704200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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