Variant report

Variant	rs1468053
Chromosome Location	chr6:134011159-134011160
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs1000025	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10485153	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10485154	0.89[ASN][1000 genomes]
rs12203961	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12210532	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12216307	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12660662	0.82[ASN][1000 genomes]
rs12660720	0.82[ASN][1000 genomes]
rs12660957	0.90[ASN][1000 genomes]
rs12661599	0.91[ASN][1000 genomes]
rs12717184	0.97[ASN][1000 genomes]
rs13194152	0.94[ASN][1000 genomes]
rs13194345	0.93[ASN][1000 genomes]
rs13196860	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13200337	0.91[ASN][1000 genomes]
rs13203797	0.91[ASN][1000 genomes]
rs13204047	0.91[ASN][1000 genomes]
rs13205217	0.90[ASN][1000 genomes]
rs13219946	0.94[ASN][1000 genomes]
rs1468052	0.87[ASN][1000 genomes]
rs1468054	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1476382	0.87[ASN][1000 genomes]
rs17062752	0.97[ASN][1000 genomes]
rs17398008	0.97[ASN][1000 genomes]
rs17398029	0.95[ASN][1000 genomes]
rs17398113	0.97[ASN][1000 genomes]
rs17398664	0.93[ASN][1000 genomes]
rs17399159	0.90[ASN][1000 genomes]
rs17476396	0.97[ASN][1000 genomes]
rs1999756	0.80[ASN][1000 genomes]
rs2069060	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2207405	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2327380	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2327381	0.96[ASN][1000 genomes]
rs34537042	0.87[ASN][1000 genomes]
rs35317124	0.86[ASN][1000 genomes]
rs35439350	0.94[ASN][1000 genomes]
rs35470523	0.97[ASN][1000 genomes]
rs36055382	0.83[ASN][1000 genomes]
rs36092198	0.92[EUR][1000 genomes]
rs55952233	0.94[ASN][1000 genomes]
rs59635582	0.81[ASN][1000 genomes]
rs62427563	0.90[ASN][1000 genomes]
rs62429310	0.96[ASN][1000 genomes]
rs6569896	0.97[ASN][1000 genomes]
rs6569897	0.94[EUR][1000 genomes]
rs6569898	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs68054668	0.90[ASN][1000 genomes]
rs6904690	0.94[ASN][1000 genomes]
rs6906782	0.91[ASN][1000 genomes]
rs6917316	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6918525	0.91[ASN][1000 genomes]
rs6918884	0.91[ASN][1000 genomes]
rs6921832	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6925029	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6926195	0.90[ASN][1000 genomes]
rs6939216	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6941465	0.91[ASN][1000 genomes]
rs71576327	0.87[ASN][1000 genomes]
rs736572	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs766996	0.91[ASN][1000 genomes]
rs7739052	0.85[EUR][1000 genomes]
rs7739104	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7739428	0.90[ASN][1000 genomes]
rs7739826	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7749675	0.86[ASN][1000 genomes]
rs7767765	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9321411	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9321412	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9493690	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9493692	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9493695	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9493698	0.94[EUR][1000 genomes]
rs9493710	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9493712	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9493716	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9493719	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032687	chr6:133987372-134059728	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1024201	chr6:133987372-134062162	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830812	chr6:133993897-134165407	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:134002400-134012800	Weak transcription	Ovary	ovary
2	chr6:134002400-134028600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:134005400-134018800	Weak transcription	Fetal Stomach	stomach
4	chr6:134011000-134011400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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