Variant report

Variant	rs3808138
Chromosome Location	chr7:126615249-126615250
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1010517	0.96[CEU][hapmap]
rs10234281	0.96[CEU][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10236120	0.89[CEU][hapmap]
rs10236204	0.96[CEU][hapmap]
rs10236227	0.92[CEU][hapmap]
rs10275501	1.00[CEU][hapmap]
rs10487463	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1155597	0.89[ASN][1000 genomes]
rs1155656	0.83[ASN][1000 genomes]
rs11563513	0.92[CEU][hapmap]
rs11563801	1.00[CEU][hapmap]
rs1204563	0.83[ASN][1000 genomes]
rs1204569	0.81[ASN][1000 genomes]
rs12164089	0.89[CEU][hapmap]
rs1361965	0.96[CEU][hapmap]
rs1361968	0.96[CEU][hapmap]
rs1361975	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1419438	0.96[CEU][hapmap]
rs1419468	0.96[CEU][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1419469	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1419470	0.96[CEU][hapmap];0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1419471	0.96[CEU][hapmap]
rs1582255	0.85[CEU][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2022072	0.96[CEU][hapmap]
rs2067052	0.86[ASN][1000 genomes]
rs2072416	0.83[ASN][1000 genomes]
rs2106188	0.83[CEU][hapmap]
rs2106189	0.96[CEU][hapmap]
rs2188188	0.96[CEU][hapmap]
rs2237776	1.00[CEU][hapmap]
rs2518954	0.83[ASN][1000 genomes]
rs2535944	0.83[ASN][1000 genomes]
rs3808136	1.00[CEU][hapmap]
rs3808142	0.96[CEU][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4540333	0.89[CEU][hapmap]
rs4728057	0.96[CEU][hapmap]
rs6950713	0.96[CEU][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[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	esv2758132	chr7:126494789-126677843	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2759562	chr7:126494789-126677843	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv427805	chr7:126494789-126677843	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv831121	chr7:126593363-126774413	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	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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