Variant report

Variant	rs7301676
Chromosome Location	chr12:44894312-44894313
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10506251	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10506252	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11612950	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11613236	1.00[ASN][1000 genomes]
rs11615599	1.00[ASN][1000 genomes]
rs17094881	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17094886	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17094892	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17571971	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17572590	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17572765	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17574492	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17649873	1.00[ASN][1000 genomes]
rs17650849	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17652715	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4768061	1.00[ASN][1000 genomes]
rs4768068	1.00[ASN][1000 genomes]
rs4768070	1.00[ASN][1000 genomes]
rs4768561	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4768566	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6582512	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7135950	1.00[ASN][1000 genomes]
rs7296595	1.00[ASN][1000 genomes]
rs7305652	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs73282400	1.00[ASN][1000 genomes]
rs73284070	1.00[ASN][1000 genomes]
rs7955981	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7957292	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7966845	1.00[ASN][1000 genomes]
rs7967221	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7974472	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7976217	1.00[CHB][hapmap];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	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	chr12:44894000-44894600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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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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