Variant report

Variant	rs561326
Chromosome Location	chr1:170138633-170138634
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10800500	0.83[CHB][hapmap]
rs10800502	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10800505	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10800506	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10919306	0.83[CHB][hapmap];0.80[ASN][1000 genomes]
rs10919307	0.81[CHB][hapmap];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10919309	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10919312	0.84[ASN][1000 genomes]
rs10919321	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10919322	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10919324	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11484822	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11484824	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12039113	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12569092	0.84[ASN][1000 genomes]
rs12751063	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2901341	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35081369	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4332407	0.83[CHB][hapmap];0.80[ASN][1000 genomes]
rs477960	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs480667	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs495127	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs519459	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs533666	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs550575	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs562931	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs569357	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6427234	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6427235	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6427236	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6669514	0.84[ASN][1000 genomes]
rs7544677	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014033	chr1:169968488-170453021	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
2	nsv535200	chr1:169968488-170453021	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
3	nsv999310	chr1:170065943-170223350	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
4	nsv3454	chr1:170134880-170149447	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:170132400-170140200	Weak transcription	Right Ventricle	heart
2	chr1:170132800-170140600	Weak transcription	Fetal Heart	heart

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