Variant report

Variant	rs679891
Chromosome Location	chr18:40427497-40427498
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10502802	0.93[CEU][hapmap]
rs12606859	0.81[CHD][hapmap]
rs16976979	0.93[CEU][hapmap]
rs16976993	0.93[CEU][hapmap]
rs16977004	0.93[CEU][hapmap]
rs16977056	1.00[CEU][hapmap];0.83[TSI][hapmap];0.94[EUR][1000 genomes]
rs16977074	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs17634039	0.93[CEU][hapmap];0.88[EUR][1000 genomes]
rs17634573	0.93[CEU][hapmap]
rs17634648	0.93[CEU][hapmap]
rs17635398	1.00[CEU][hapmap]
rs17635858	1.00[CEU][hapmap];0.83[TSI][hapmap];0.94[EUR][1000 genomes]
rs17712687	0.93[CEU][hapmap]
rs17712831	0.93[CEU][hapmap];0.93[EUR][1000 genomes]
rs17713111	0.93[CEU][hapmap]
rs17713637	1.00[CEU][hapmap]
rs17713884	0.86[CEU][hapmap];0.94[EUR][1000 genomes]
rs17714417	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs17714864	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs1943946	0.94[ASW][hapmap];0.93[CEU][hapmap];0.81[CHB][hapmap];0.91[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap]
rs1944413	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs41444547	1.00[CEU][hapmap];0.83[TSI][hapmap];0.93[EUR][1000 genomes]
rs473976	0.94[ASW][hapmap];1.00[CEU][hapmap];0.87[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs482472	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs488136	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];0.95[MEX][hapmap];0.92[MKK][hapmap];0.96[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4890240	0.92[EUR][1000 genomes]
rs4890241	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs4890411	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs4890412	0.93[EUR][1000 genomes]
rs4890413	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs4890414	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs4890416	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs4890417	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs531438	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs549415	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs551291	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.89[MKK][hapmap];0.97[TSI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61111721	0.90[EUR][1000 genomes]
rs630915	0.87[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs632168	0.87[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs649056	0.88[ASW][hapmap];1.00[CEU][hapmap];0.87[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs684446	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7230586	0.92[EUR][1000 genomes]
rs7231491	0.93[CEU][hapmap]
rs73470101	0.94[EUR][1000 genomes]
rs73471605	0.94[EUR][1000 genomes]
rs73471620	0.93[EUR][1000 genomes]
rs73471624	0.93[EUR][1000 genomes]
rs73471626	0.93[EUR][1000 genomes]
rs73471636	0.93[EUR][1000 genomes]
rs73471638	0.93[EUR][1000 genomes]
rs73471646	0.93[EUR][1000 genomes]
rs73471654	0.90[EUR][1000 genomes]
rs73471657	0.93[EUR][1000 genomes]
rs73471679	0.90[EUR][1000 genomes]
rs8084102	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs8085172	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs8087737	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs8088192	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs8088908	1.00[CEU][hapmap]
rs8089316	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs8091455	0.91[EUR][1000 genomes]
rs8091643	0.86[CEU][hapmap];0.91[EUR][1000 genomes]
rs8092263	0.89[EUR][1000 genomes]
rs8093580	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs8093756	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs8094360	0.93[CEU][hapmap];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1056794	chr18:40197837-40688514	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv3331556	chr18:40424054-40427652	ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:40424800-40434800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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