Variant report

Variant	rs9635173
Chromosome Location	chr14:63283414-63283415
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1003309	0.85[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1072022	0.91[CHD][hapmap];0.89[JPT][hapmap];0.88[ASN][1000 genomes]
rs10747298	0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.92[ASN][1000 genomes]
rs11158453	0.85[CHB][hapmap];0.90[JPT][hapmap];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11158454	0.85[CEU][hapmap];0.90[EUR][1000 genomes]
rs11846728	0.81[EUR][1000 genomes]
rs12431779	0.90[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.90[ASN][1000 genomes]
rs12435061	0.82[CEU][hapmap]
rs12435655	0.82[CEU][hapmap]
rs12436815	0.81[CHB][hapmap];0.84[CHD][hapmap]
rs12881113	0.81[CHB][hapmap]
rs12882073	0.84[CHB][hapmap];0.85[JPT][hapmap]
rs12882869	0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap]
rs12883427	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1475743	0.85[CEU][hapmap];0.90[EUR][1000 genomes]
rs1475744	0.90[EUR][1000 genomes]
rs1490025	0.82[CEU][hapmap]
rs1844510	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs1884509	0.86[CHB][hapmap];0.89[CHD][hapmap];0.83[GIH][hapmap]
rs2016794	0.82[CEU][hapmap]
rs2355733	0.85[CHB][hapmap];0.84[JPT][hapmap]
rs2355734	0.91[ASN][1000 genomes]
rs4271527	0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs4902186	0.83[GIH][hapmap]
rs4902187	0.85[CEU][hapmap];0.87[GIH][hapmap];0.90[EUR][1000 genomes]
rs4902188	0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs8011235	0.84[CHB][hapmap];0.90[JPT][hapmap];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8014674	0.87[GIH][hapmap]
rs8016650	0.85[EUR][1000 genomes]
rs9635174	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902015	chr14:63261862-63356253	Enhancers Weak transcription ZNF genes & repeats Strong transcription	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
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