Variant report

Variant	rs12703916
Chromosome Location	chr7:147164089-147164090
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10239776	1.00[CHB][hapmap]
rs10251488	1.00[CHB][hapmap]
rs10276658	1.00[CHB][hapmap]
rs10500175	1.00[CHB][hapmap]
rs10500185	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10500187	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11505677	1.00[CHB][hapmap]
rs11764538	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11770339	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11771144	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11772135	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs11773547	1.00[CHB][hapmap]
rs11773683	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12703909	0.84[CEU][hapmap]
rs12703911	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs12703921	1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12703922	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs13221396	1.00[CEU][hapmap]
rs13221977	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs13222223	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13223092	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13224673	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs13227291	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs13229651	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs13231364	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs13231991	0.95[CEU][hapmap];1.00[CHB][hapmap];0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13233234	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13234094	1.00[CHB][hapmap]
rs13234757	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs13235407	1.00[CHB][hapmap]
rs13235593	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13238470	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs13241063	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13242678	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13243643	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13246604	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13246788	0.93[CEU][hapmap];1.00[CHB][hapmap]
rs13247132	0.90[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13247289	0.82[CEU][hapmap]
rs1357896	1.00[CHB][hapmap]
rs1404711	1.00[CHB][hapmap]
rs1406288	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1528520	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17170636	1.00[CHB][hapmap]
rs17223460	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs17224658	0.92[CEU][hapmap];1.00[CHB][hapmap]
rs17498276	1.00[CHB][hapmap]
rs1842273	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1842274	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1860135	1.00[CHB][hapmap]
rs1871492	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1990251	1.00[CHB][hapmap]
rs2046052	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs2373031	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2373128	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs2373129	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs34163397	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34959888	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34993596	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35288063	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35696201	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35756055	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35894873	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35894927	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36103173	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4272288	1.00[CHB][hapmap]
rs5028055	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs6947112	1.00[CHB][hapmap]
rs6951143	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs6955567	1.00[CHB][hapmap]
rs6957443	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6979164	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs71530784	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs747138	0.92[CEU][hapmap];1.00[CHB][hapmap]
rs7781464	1.00[CHB][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7788405	1.00[CHB][hapmap]
rs7810103	1.00[CHB][hapmap]
rs872714	1.00[CEU][hapmap]
rs957484	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs997223	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[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	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 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
chromosomal regions: chr1:12345-34567

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