Variant report

Variant	rs7304503
Chromosome Location	chr12:44846775-44846776
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11182500	0.96[EUR][1000 genomes]
rs11610751	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11611513	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11612006	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11613516	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11837624	1.00[ASN][1000 genomes]
rs1353144	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1493758	1.00[ASN][1000 genomes]
rs17094591	0.94[EUR][1000 genomes]
rs17094614	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17094655	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17094666	1.00[ASN][1000 genomes]
rs1817884	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1873977	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1873979	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55636254	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs55726837	1.00[ASN][1000 genomes]
rs56367710	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57180808	1.00[EUR][1000 genomes]
rs73092522	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73092524	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7309287	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73094350	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73094362	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73094373	1.00[EUR][1000 genomes]
rs73276296	1.00[ASN][1000 genomes]
rs73276299	1.00[ASN][1000 genomes]
rs765530	1.00[EUR][1000 genomes]
rs869629	0.80[AMR][1000 genomes];0.94[EUR][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	nsv1049818	chr12:44486312-45133783	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44840600-44848200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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