Variant report

Variant	rs12703921
Chromosome Location	chr7:147189187-147189188
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

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[CHB][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10500187	1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs11505677	1.00[CHB][hapmap]
rs11764538	1.00[CHB][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11770339	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11771144	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11772135	1.00[CHB][hapmap]
rs11773547	1.00[CHB][hapmap]
rs11773683	1.00[CHB][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12703911	1.00[CHB][hapmap]
rs12703916	1.00[CHB][hapmap]
rs12703922	1.00[CHB][hapmap]
rs13221977	1.00[CHB][hapmap]
rs13222223	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13223092	1.00[ASN][1000 genomes]
rs13224673	1.00[CHB][hapmap]
rs13227291	1.00[CHB][hapmap]
rs13229651	1.00[CHB][hapmap]
rs13231364	1.00[CHB][hapmap]
rs13231991	1.00[CHB][hapmap];0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13233234	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs13234094	1.00[CHB][hapmap]
rs13234757	1.00[CHB][hapmap]
rs13235407	1.00[CHB][hapmap]
rs13235593	1.00[CHB][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13238470	1.00[CHB][hapmap]
rs13241063	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13242678	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13243643	0.86[AFR][1000 genomes]
rs13246604	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13246788	1.00[CHB][hapmap]
rs13247132	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1357896	1.00[CHB][hapmap]
rs1404711	1.00[CHB][hapmap]
rs1406288	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1528520	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17170636	1.00[CHB][hapmap]
rs17223460	1.00[CHB][hapmap]
rs17224658	1.00[CHB][hapmap]
rs17498276	1.00[CHB][hapmap]
rs1842273	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1842274	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1860135	1.00[CHB][hapmap]
rs1871492	1.00[CHB][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1990251	1.00[CHB][hapmap]
rs2046052	1.00[CHB][hapmap]
rs2373031	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2373128	1.00[CHB][hapmap]
rs2373129	1.00[CHB][hapmap]
rs34163397	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34959888	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34993596	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35288063	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs35696201	0.86[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35756055	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35894873	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35894927	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36103173	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4272288	1.00[CHB][hapmap]
rs5028055	1.00[CHB][hapmap]
rs6947112	1.00[CHB][hapmap]
rs6951143	1.00[CHB][hapmap]
rs6955567	1.00[CHB][hapmap]
rs6957443	1.00[AFR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6979164	1.00[CHB][hapmap]
rs747138	1.00[CHB][hapmap]
rs7779279	1.00[CHB][hapmap]
rs7781464	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7788405	1.00[CHB][hapmap]
rs7810103	1.00[CHB][hapmap]
rs957484	1.00[CHB][hapmap]
rs997223	1.00[CHB][hapmap];1.00[AFR][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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147188600-147191200	Enhancers	Muscle Satellite Cultured Cells	--
2	chr7:147188800-147191200	Enhancers	Osteobl	bone

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