Variant report

Variant	rs73858573
Chromosome Location	chr3:99235368-99235369
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs58223529	0.83[AFR][1000 genomes]
rs59106684	1.00[AMR][1000 genomes]
rs59832918	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858442	1.00[AMR][1000 genomes]
rs73858445	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858446	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858448	0.92[AFR][1000 genomes]
rs73858453	0.92[AFR][1000 genomes]
rs73858456	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858458	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858459	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858570	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858571	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858576	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858577	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73858805	1.00[AMR][1000 genomes]
rs73858844	1.00[AMR][1000 genomes]
rs73858850	1.00[AMR][1000 genomes]
rs73861422	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7627465	1.00[AMR][1000 genomes]
rs7641113	1.00[AMR][1000 genomes]
rs7652601	1.00[AMR][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	nsv1007486	chr3:98597738-99249081	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv530026	chr3:98837320-99340537	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3422853	chr3:99208019-99342748	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:99228400-99243000	Weak transcription	Aorta	Aorta
2	chr3:99233000-99237800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:99234200-99235600	Enhancers	HUVEC	blood vessel

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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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