Variant report

Variant	rs1540478
Chromosome Location	chr4:173661525-173661526
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10014796	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10016257	0.91[CEU][hapmap]
rs10050292	0.91[CEU][hapmap]
rs10213357	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10222748	0.96[CEU][hapmap];0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11132960	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11729518	0.86[CEU][hapmap];0.94[EUR][1000 genomes]
rs11734921	0.80[CEU][hapmap]
rs11735233	0.88[CEU][hapmap]
rs13104048	0.84[CEU][hapmap]
rs13134091	0.95[EUR][1000 genomes]
rs13138074	0.84[CEU][hapmap]
rs1370576	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs1370577	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs1437845	0.87[CEU][hapmap];0.94[EUR][1000 genomes]
rs1437854	0.87[CEU][hapmap]
rs1437856	0.91[CEU][hapmap]
rs1540473	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1540474	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs1540475	0.89[CEU][hapmap]
rs1540476	0.85[CEU][hapmap]
rs1561305	0.91[CEU][hapmap]
rs1561306	0.91[CEU][hapmap]
rs1561307	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs1595413	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17052104	0.84[CEU][hapmap]
rs1821862	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs1837132	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2043780	0.87[CEU][hapmap]
rs2083136	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs2118443	0.96[CEU][hapmap];1.00[YRI][hapmap]
rs28552483	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28579160	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28727534	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28767047	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34364219	0.94[EUR][1000 genomes]
rs35170073	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4100737	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs4315754	0.95[CEU][hapmap];0.81[YRI][hapmap]
rs4396969	0.91[CEU][hapmap]
rs4414931	0.91[CEU][hapmap]
rs4423855	0.96[CEU][hapmap];1.00[YRI][hapmap]
rs4572851	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs6553647	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs6553648	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67168311	0.95[EUR][1000 genomes]
rs6822057	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6830773	0.87[CEU][hapmap]
rs6841156	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs6853969	0.93[EUR][1000 genomes]
rs716645	0.95[CEU][hapmap]
rs716646	0.91[CEU][hapmap]
rs716647	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs7669486	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7674050	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs7677835	0.83[CEU][hapmap];0.84[EUR][1000 genomes]
rs9312528	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs9992901	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9995075	1.00[CEU][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031592	chr4:173112542-173662991	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv537359	chr4:173112542-173662991	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv948856	chr4:173388217-173967546	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv949126	chr4:173466221-174051451	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv880685	chr4:173562564-173661711	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv880613	chr4:173569281-173661711	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv3327952	chr4:173591786-173805861	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 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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