Variant report

Variant	rs732719
Chromosome Location	chr14:79012652-79012653
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10144398	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap]
rs1030122	0.96[CEU][hapmap];0.81[CHB][hapmap];0.93[JPT][hapmap]
rs11159371	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11159372	0.80[EUR][1000 genomes]
rs11624601	0.81[EUR][1000 genomes]
rs12587931	0.95[CEU][hapmap];0.85[CHB][hapmap];0.92[JPT][hapmap]
rs12883210	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2032747	0.87[CEU][hapmap]
rs2370824	1.00[CEU][hapmap];0.85[CHB][hapmap];0.85[JPT][hapmap]
rs4899717	0.96[CEU][hapmap];0.85[CHB][hapmap];0.93[JPT][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4903778	0.96[CEU][hapmap];0.81[CHB][hapmap];0.93[JPT][hapmap]
rs59241723	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7141909	0.80[EUR][1000 genomes]
rs724622	0.95[CEU][hapmap];0.80[CHB][hapmap];0.92[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs741523	0.82[CHB][hapmap];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8003897	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs8006051	0.95[CEU][hapmap];0.85[CHB][hapmap];0.92[JPT][hapmap]
rs8011361	1.00[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760000	chr14:78875607-79173528	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2758363	chr14:78903610-79173528	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1037999	chr14:78966643-79026875	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv565235	chr14:78978181-79027504	Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3359167	chr14:79012345-79012802	Enhancers	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79012600-79013400	Enhancers	HUES48 Cell Line	embryonic stem cell

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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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