Variant report

Variant	rs2093599
Chromosome Location	chr13:53747011-53747012
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1016829	0.80[ASN][1000 genomes]
rs1322938	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1322939	0.88[AFR][1000 genomes]
rs1322941	0.86[EUR][1000 genomes]
rs1322942	0.87[EUR][1000 genomes]
rs1322943	0.87[EUR][1000 genomes]
rs1322944	0.87[EUR][1000 genomes]
rs1322949	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1322951	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1322952	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1322955	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1322956	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1322961	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1322962	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1343602	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1407685	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1419218	0.87[EUR][1000 genomes]
rs1853369	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1909648	0.82[EUR][1000 genomes]
rs1923767	0.87[EUR][1000 genomes]
rs1923768	0.87[EUR][1000 genomes]
rs1923771	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1951722	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2015677	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2038649	0.84[EUR][1000 genomes]
rs2093598	0.87[EUR][1000 genomes]
rs2408766	0.82[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs2491124	0.80[ASN][1000 genomes]
rs2759675	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2759706	0.80[ASN][1000 genomes]
rs2759708	0.85[EUR][1000 genomes]
rs2759709	0.82[EUR][1000 genomes]
rs2759712	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2759716	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2806936	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2806939	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2806941	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2806956	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2806960	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2806963	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2806964	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2806966	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4886202	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4886270	0.86[ASN][1000 genomes]
rs7994915	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8002513	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs912052	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs912054	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs927518	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9527057	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9536358	0.86[EUR][1000 genomes]
rs9536359	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9536363	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9568807	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9568813	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9568826	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs959222	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]

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	nsv1050969	chr13:53665927-54064861	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	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	chr13:53745400-53750600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:53745800-53748800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr13:53746000-53748600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr13:53746200-53748200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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