Variant report

Variant	rs6810225
Chromosome Location	chr3:85503497-85503498
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs1014796	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1030720	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10433499	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10511078	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10865609	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes]
rs10865611	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11127898	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11714549	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes]
rs12054328	1.00[JPT][hapmap]
rs12487446	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12491352	0.82[JPT][hapmap]
rs12491707	1.00[JPT][hapmap]
rs12492753	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12494446	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12498133	1.00[JPT][hapmap]
rs12629607	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12631046	0.85[EUR][1000 genomes]
rs12638798	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12639001	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12639564	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1368744	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1368747	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1375566	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1433710	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes]
rs1433713	1.00[CEU][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1449386	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1449401	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1449403	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1465716	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes]
rs1594795	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17023019	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17023032	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1900916	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1992967	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2017293	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2029134	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2044725	1.00[JPT][hapmap]
rs2053105	0.86[AMR][1000 genomes]
rs2077839	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2163970	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs2167043	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2326319	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4856270	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4856274	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4856278	1.00[CHB][hapmap]
rs4856568	0.82[JPT][hapmap]
rs4856582	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4856584	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs62250710	0.85[EUR][1000 genomes]
rs6549027	0.85[EUR][1000 genomes]
rs6772750	0.92[AMR][1000 genomes]
rs6778223	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6781515	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6807666	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6809486	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs726610	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs734298	0.84[AMR][1000 genomes]
rs7618494	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7623369	0.92[AMR][1000 genomes]
rs7623474	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7623947	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7640828	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7647981	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7651113	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7652808	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs892365	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9309974	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9309978	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes]
rs9824071	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9824386	0.86[AMR][1000 genomes]
rs9824840	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9825345	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9831848	0.84[AMR][1000 genomes]
rs9833972	1.00[JPT][hapmap]
rs9843953	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs9846153	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9869121	0.84[AMR][1000 genomes]
rs9873752	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9879417	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9990095	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3419993	chr3:85030343-85663403	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
2	esv2753915	chr3:85071410-85624810	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1002238	chr3:85357855-85719373	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
4	nsv536619	chr3:85357855-85719373	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1004254	chr3:85394816-85514910	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
6	nsv536621	chr3:85394816-85514910	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
7	nsv590904	chr3:85438564-85551403	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv590905	chr3:85438564-85797093	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv998829	chr3:85449960-85641099	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv536622	chr3:85449960-85641099	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv526621	chr3:85470642-85667683	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv1009512	chr3:85472690-85533487	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
13	nsv536623	chr3:85472690-85533487	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
14	nsv522784	chr3:85480724-85507231	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
15	nsv1013601	chr3:85489536-85570465	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
16	nsv536624	chr3:85489536-85570465	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
17	nsv1009927	chr3:85497666-85669155	Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	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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