Variant report

Variant	rs4743338
Chromosome Location	chr9:102044553-102044554
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1032835	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs151169	0.90[CHB][hapmap];0.94[ASN][1000 genomes]
rs162616	0.96[ASN][1000 genomes]
rs162623	0.89[ASN][1000 genomes]
rs162629	0.90[CHB][hapmap];0.82[JPT][hapmap];0.94[ASN][1000 genomes]
rs162630	0.83[ASN][1000 genomes]
rs1648641	0.91[ASN][1000 genomes]
rs1746155	0.89[ASN][1000 genomes]
rs184437	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs189042	1.00[CHB][hapmap];0.82[JPT][hapmap];0.96[ASN][1000 genomes]
rs193021	0.90[CHB][hapmap];0.82[JPT][hapmap];0.94[ASN][1000 genomes]
rs2114429	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2900576	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs383602	1.00[ASN][1000 genomes]
rs405952	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs418919	0.94[ASN][1000 genomes]
rs433706	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs449188	1.00[ASN][1000 genomes]
rs4579588	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap]
rs4742765	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4743336	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs504640	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs526102	1.00[ASN][1000 genomes]
rs56408008	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57418404	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58111537	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58132610	0.85[ASN][1000 genomes]
rs692905	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs701366	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs701371	1.00[ASN][1000 genomes]
rs7025649	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7031176	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7031193	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7048711	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][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	nsv893620	chr9:102029791-102194921	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3508544	chr9:102042381-102045079	Inactive region	TF binding region	1 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
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