Variant report

Variant	rs16871115
Chromosome Location	chr4:21476783-21476784
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10516385	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10516388	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs10516389	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13101628	0.92[ASN][1000 genomes]
rs13103191	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs13104819	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13108860	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13109655	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13109855	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13121386	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs13122564	0.93[ASN][1000 genomes]
rs13122807	0.93[ASN][1000 genomes]
rs13129501	0.92[ASN][1000 genomes]
rs13129942	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs13129962	0.89[ASN][1000 genomes]
rs13135994	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13136002	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13137136	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs13143135	1.00[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs13144924	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13145622	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs13148416	0.87[ASN][1000 genomes]
rs1495501	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1495502	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1495503	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16871123	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16871156	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17464578	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17464752	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17464793	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17464828	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs17465022	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17465591	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17523841	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17523876	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs17524637	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17524672	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs17524714	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs17524784	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs17524952	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs17525063	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2874930	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2874931	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34222306	0.93[ASN][1000 genomes]
rs34339769	0.90[ASN][1000 genomes]
rs35032154	0.93[ASN][1000 genomes]
rs35733464	1.00[ASN][1000 genomes]
rs35895330	0.93[ASN][1000 genomes]
rs58751863	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs66601179	0.93[ASN][1000 genomes]
rs67306339	0.93[ASN][1000 genomes]
rs68049217	0.93[ASN][1000 genomes]
rs68116688	0.93[ASN][1000 genomes]
rs71607078	0.93[ASN][1000 genomes]
rs73252219	0.93[ASN][1000 genomes]
rs7441592	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9685466	1.00[CHB][hapmap];1.00[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	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1014062	chr4:21270358-21479027	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv829879	chr4:21418568-21611002	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
4	nsv998481	chr4:21421945-21608805	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
5	nsv593804	chr4:21469139-21477084	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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