Variant report

Variant	rs7328151
Chromosome Location	chr13:53953549-53953550
allele	A/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:33)

rs_ID	r²[population]
rs1156006	0.85[ASN][1000 genomes]
rs11618497	0.97[ASN][1000 genomes]
rs1342669	0.99[ASN][1000 genomes]
rs1373273	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1373276	0.98[ASN][1000 genomes]
rs1373277	0.86[ASN][1000 genomes]
rs1373281	1.00[ASN][1000 genomes]
rs1418617	0.86[ASN][1000 genomes]
rs1443905	0.98[ASN][1000 genomes]
rs1443908	0.82[ASN][1000 genomes]
rs2165985	0.92[ASN][1000 genomes]
rs2408858	0.94[ASN][1000 genomes]
rs2813573	1.00[ASN][1000 genomes]
rs4883678	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4884411	0.86[ASN][1000 genomes]
rs7322098	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7329909	0.94[ASN][1000 genomes]
rs7332332	0.82[ASN][1000 genomes]
rs7985119	0.98[ASN][1000 genomes]
rs7987501	0.83[ASN][1000 genomes]
rs7992723	0.86[CHB][hapmap]
rs8001044	0.98[ASN][1000 genomes]
rs8002970	0.98[ASN][1000 genomes]
rs9316613	0.99[ASN][1000 genomes]
rs9527077	0.82[ASN][1000 genomes]
rs9536405	0.99[ASN][1000 genomes]
rs9536406	0.99[ASN][1000 genomes]
rs9536410	0.82[ASN][1000 genomes]
rs9536411	0.82[ASN][1000 genomes]
rs9568838	0.85[ASN][1000 genomes]
rs9568839	0.85[ASN][1000 genomes]
rs9568848	0.82[ASN][1000 genomes]
rs9596807	0.83[ASN][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	nsv1050969	chr13:53665927-54064861	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1040236	chr13:53928195-53955060	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1051184	chr13:53928195-53956469	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:53953200-53954600	Enhancers	Liver	Liver

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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