Variant report

Variant	rs1689270
Chromosome Location	chr1:76390937-76390938
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs1001160	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10873797	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11161699	0.84[AFR][1000 genomes]
rs11161848	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11161887	0.84[CEU][hapmap]
rs11161902	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1146631	1.00[JPT][hapmap]
rs1146634	1.00[JPT][hapmap]
rs1146636	1.00[JPT][hapmap]
rs1146644	1.00[JPT][hapmap]
rs11578480	0.91[CEU][hapmap];1.00[JPT][hapmap]
rs11588643	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs1159215	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12043473	1.00[JPT][hapmap]
rs12130832	0.96[CEU][hapmap];1.00[JPT][hapmap]
rs12138898	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12142247	0.96[CEU][hapmap];1.00[JPT][hapmap]
rs1250876	0.84[CEU][hapmap]
rs1250880	0.80[CEU][hapmap]
rs1251533	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1251584	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1303870	0.84[CEU][hapmap]
rs1463812	1.00[JPT][hapmap]
rs1498311	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs1628063	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1630302	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1630587	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17647178	0.91[CEU][hapmap];1.00[JPT][hapmap]
rs1770882	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1770889	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1796795	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1796810	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1796813	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1796815	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1796827	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1856791	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs1908089	0.84[CEU][hapmap]
rs2029682	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs5745323	1.00[JPT][hapmap]
rs5745325	0.95[CEU][hapmap];1.00[JPT][hapmap]
rs5745331	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.81[AFR][1000 genomes]
rs5745347	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs5745383	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs5745394	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs5745430	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5745523	0.84[CEU][hapmap]
rs5745543	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5745545	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5745546	0.84[CEU][hapmap]
rs5745547	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6593520	1.00[JPT][hapmap]
rs6593521	1.00[JPT][hapmap]
rs6656501	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs721204	1.00[JPT][hapmap]
rs7516477	0.84[CEU][hapmap]
rs879268	1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[ASN][1000 genomes]

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	nsv1014072	chr1:76200531-76460726	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv535005	chr1:76200531-76460726	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv1004669	chr1:76301198-76409451	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv871671	chr1:76304215-76391646	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv998499	chr1:76361784-76598712	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 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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