Variant report

Variant	rs73097874
Chromosome Location	chr3:60904499-60904500
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs17632419	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs17632681	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17683604	0.94[AMR][1000 genomes]
rs2594130	0.85[EUR][1000 genomes]
rs55932127	0.80[EUR][1000 genomes]
rs56259187	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6782282	0.80[EUR][1000 genomes]
rs6807024	0.80[EUR][1000 genomes]
rs717292	0.80[EUR][1000 genomes]
rs73092711	0.83[EUR][1000 genomes]
rs73092730	0.85[EUR][1000 genomes]
rs73097817	0.94[AMR][1000 genomes]
rs73111744	0.80[EUR][1000 genomes]
rs73111751	0.80[EUR][1000 genomes]
rs73111752	0.80[EUR][1000 genomes]
rs73111756	0.83[EUR][1000 genomes]
rs7626938	0.80[EUR][1000 genomes]

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	nsv534038	chr3:60781917-60993082	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2757872	chr3:60781943-61019003	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2759152	chr3:60781943-61220809	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive 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	chr3:60902600-60906600	Weak transcription	Adipose Derived Mesenchymal Stem Cell 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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