Variant report

Variant	rs9789430
Chromosome Location	chr2:142672764-142672765
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10165154	0.91[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs10181838	0.96[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap]
rs10182288	0.96[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs10183142	1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs10190657	0.92[ASN][1000 genomes]
rs10194554	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10198650	0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10496906	0.93[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap]
rs11693445	1.00[JPT][hapmap]
rs11884984	0.85[CEU][hapmap];0.86[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11895935	0.89[ASN][1000 genomes]
rs12467014	0.96[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap]
rs12471235	0.96[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap]
rs12611498	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12611558	0.91[CHB][hapmap];0.89[JPT][hapmap];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12618005	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12618032	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12621414	0.91[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12623563	0.96[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes]
rs12691627	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs12995397	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs13011272	1.00[YRI][hapmap]
rs13012265	0.93[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs13013316	0.86[JPT][hapmap]
rs13024435	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13031056	0.96[CEU][hapmap];0.92[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.82[AMR][1000 genomes]
rs13408365	0.91[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs13418027	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs13429414	0.93[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1369528	0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1369530	0.96[CEU][hapmap];1.00[JPT][hapmap]
rs1369542	0.91[CHB][hapmap];0.86[JPT][hapmap]
rs1435598	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs1435612	0.96[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap]
rs1435616	0.96[CEU][hapmap];0.92[CHB][hapmap];0.86[JPT][hapmap]
rs1529869	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs1561019	0.93[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs16847640	0.84[CHB][hapmap]
rs1898018	0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1991997	0.92[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1991998	0.93[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2196353	0.96[CEU][hapmap];0.92[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap]
rs2381169	1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs34879655	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4662555	0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4662557	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6429927	0.91[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7421755	0.83[YRI][hapmap]
rs7579772	0.96[CEU][hapmap];1.00[JPT][hapmap]
rs7593594	0.93[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7602677	0.83[CHB][hapmap]
rs9287326	0.96[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs960219	1.00[YRI][hapmap]

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	nsv530398	chr2:142474842-142843839	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv583238	chr2:142646363-142739121	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv875251	chr2:142656200-142701852	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	n/a
4	nsv875252	chr2:142666003-142768518	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 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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