Variant report

Variant	rs10520234
Chromosome Location	chr4:173347371-173347372
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10016863	0.80[ASN][1000 genomes]
rs10017948	0.82[CHD][hapmap];0.95[JPT][hapmap];0.81[TSI][hapmap]
rs10018148	0.87[GIH][hapmap];0.95[JPT][hapmap]
rs10866354	0.93[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap]
rs11132943	0.87[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12644293	0.91[MEX][hapmap];0.90[MKK][hapmap]
rs13116631	0.93[LWK][hapmap];0.95[YRI][hapmap]
rs1396220	0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs1508259	0.89[YRI][hapmap]
rs1508260	0.81[ASW][hapmap];0.87[CEU][hapmap];0.84[CHB][hapmap];0.88[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.92[LWK][hapmap];0.82[MEX][hapmap];0.83[TSI][hapmap];0.85[YRI][hapmap]
rs17058545	0.81[MEX][hapmap]
rs2200257	0.82[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap]
rs2654774	0.85[CEU][hapmap]
rs2661806	0.84[CEU][hapmap]
rs6553634	0.91[MEX][hapmap]
rs6823609	0.95[JPT][hapmap]
rs6852501	0.87[CEU][hapmap];0.84[CHB][hapmap];0.88[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap];0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7680231	0.87[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.85[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	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	nsv534293	chr4:173121379-173606082	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv880416	chr4:173287422-173388217	Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1031327	chr4:173306405-173465248	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 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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