Variant report

Variant	rs9561151
Chromosome Location	chr13:93436706-93436707
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs12428589	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12429124	0.84[AMR][1000 genomes]
rs12429680	1.00[CHB][hapmap];0.84[JPT][hapmap]
rs12430678	0.94[AMR][1000 genomes]
rs12431303	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs1590556	0.94[ASN][1000 genomes]
rs1890198	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1933194	0.81[CHB][hapmap]
rs1999857	0.81[CHB][hapmap]
rs2031585	1.00[CHB][hapmap]
rs2148225	1.00[CHB][hapmap]
rs2182367	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs35226443	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7333121	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7334046	0.81[CHB][hapmap]
rs7338330	0.81[CHB][hapmap]
rs7338542	0.81[CHB][hapmap]
rs7491566	0.81[CHB][hapmap]
rs7984465	0.91[ASN][1000 genomes]
rs7987140	0.81[CHB][hapmap]
rs7988257	1.00[CHB][hapmap]
rs7992127	0.81[CHB][hapmap]
rs8000315	1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9301832	0.81[CHB][hapmap]
rs9556205	0.89[AMR][1000 genomes]
rs9556206	0.86[CHB][hapmap]
rs9556211	0.86[CHB][hapmap]
rs9556215	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9556216	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9556217	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9556218	1.00[CHB][hapmap];0.84[JPT][hapmap];0.94[ASN][1000 genomes]
rs9556219	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs9556222	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs9556224	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9556227	1.00[CHB][hapmap];0.93[JPT][hapmap];0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9556228	1.00[CHB][hapmap];0.85[JPT][hapmap];0.91[ASN][1000 genomes]
rs9556229	1.00[CHB][hapmap];0.84[JPT][hapmap]
rs9561124	0.81[CHB][hapmap]
rs9561130	0.81[CHB][hapmap]
rs9561131	0.84[AMR][1000 genomes]
rs9561136	0.86[CHB][hapmap]
rs9561142	0.86[CHB][hapmap]
rs9561143	0.86[CHB][hapmap]
rs9561152	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9561163	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9561164	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9561165	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs9561166	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs9561168	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs9561169	1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9561170	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs9561172	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs9561173	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs9561175	0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9561176	0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9561177	1.00[CHB][hapmap];0.93[JPT][hapmap];0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9561178	1.00[CHB][hapmap];0.92[JPT][hapmap];0.91[ASN][1000 genomes]
rs9561179	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs9561180	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs9561181	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs9561182	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs9561183	1.00[CHB][hapmap];0.84[JPT][hapmap]

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	nsv869070	chr13:93347616-94286933	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv456072	chr13:93419362-93506864	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv562746	chr13:93419362-93506864	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

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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