Variant report

Variant	rs993776
Chromosome Location	chr4:47202476-47202477
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10001018	0.91[JPT][hapmap];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10001568	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10002370	0.82[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];0.88[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10016388	0.91[JPT][hapmap]
rs10017581	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10025913	0.82[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap]
rs10028379	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs10034675	0.93[CHB][hapmap];0.91[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10805151	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10805152	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10938473	0.91[JPT][hapmap];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10938474	0.87[JPT][hapmap]
rs10938477	0.82[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12500569	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12502432	0.82[CEU][hapmap];0.93[CHB][hapmap];0.82[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12505780	0.81[ASN][1000 genomes]
rs13105212	0.82[JPT][hapmap]
rs13117729	0.93[CHB][hapmap];0.91[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13135929	0.93[CHB][hapmap];0.91[JPT][hapmap];0.88[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1372487	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1372493	0.93[CHB][hapmap];0.91[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1372495	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1372496	0.93[CHB][hapmap];0.91[JPT][hapmap];0.88[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1442093	0.93[CHB][hapmap];0.90[JPT][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1442094	0.82[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1442095	0.93[CHB][hapmap];0.91[JPT][hapmap]
rs1442098	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1442099	0.82[JPT][hapmap]
rs1442101	0.82[JPT][hapmap]
rs1442104	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1442106	0.92[CHB][hapmap];0.91[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1542097	0.91[CEU][hapmap];0.91[JPT][hapmap];0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1561776	0.93[CHB][hapmap];0.91[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1596139	0.82[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs2044084	0.82[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs2882622	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3906823	0.82[JPT][hapmap]
rs4315750	0.91[JPT][hapmap]
rs4317179	0.91[JPT][hapmap]
rs4396968	0.82[JPT][hapmap]
rs4501194	0.82[JPT][hapmap]
rs4508858	0.93[CHB][hapmap];0.91[JPT][hapmap];0.88[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4597805	0.91[JPT][hapmap]
rs4694836	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4694837	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4695193	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4695195	0.93[CHB][hapmap];0.91[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4695196	0.93[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs6447534	0.82[JPT][hapmap]
rs6447535	0.91[JPT][hapmap];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6447536	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6447537	0.93[CHB][hapmap];0.91[JPT][hapmap]
rs6819839	0.91[JPT][hapmap]
rs6827925	0.91[JPT][hapmap];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6829206	0.84[JPT][hapmap]
rs6832403	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6839184	0.82[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap]
rs6839998	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6842392	0.93[CHB][hapmap];0.91[JPT][hapmap]
rs6846701	0.91[JPT][hapmap]
rs6847023	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6854338	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7660765	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7666212	0.82[JPT][hapmap]
rs7672580	0.93[CHB][hapmap];0.91[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7672757	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7680321	0.82[JPT][hapmap]
rs7680746	0.82[JPT][hapmap]
rs7684997	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7689895	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9762551	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs988944	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs994447	0.91[JPT][hapmap];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9991346	1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.81[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	nsv829922	chr4:47093785-47261181	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv879003	chr4:47102993-47215939	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1009766	chr4:47155845-47277391	Enhancers Flanking Active TSS Weak transcription Active TSS	lncRNA	n/a	inside rSNPs	diseases
4	nsv1013512	chr4:47178547-47213133	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
5	nsv537079	chr4:47178547-47213133	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	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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