Variant report

Variant	rs73296205
Chromosome Location	chr12:51305251-51305252
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11169614	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11835513	1.00[AMR][1000 genomes]
rs12300872	0.87[AFR][1000 genomes]
rs17124979	1.00[AMR][1000 genomes]
rs17125085	1.00[AMR][1000 genomes]
rs17125212	1.00[AMR][1000 genomes]
rs17125227	1.00[AMR][1000 genomes]
rs17125245	1.00[AMR][1000 genomes]
rs56809906	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56840343	1.00[AMR][1000 genomes]
rs56883422	1.00[AMR][1000 genomes]
rs56979742	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58343549	1.00[AMR][1000 genomes]
rs58493263	1.00[AMR][1000 genomes]
rs60089061	1.00[AMR][1000 genomes]
rs60610335	1.00[AMR][1000 genomes]
rs60720958	1.00[AMR][1000 genomes]
rs61550892	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7137990	1.00[AMR][1000 genomes]
rs7303962	1.00[AMR][1000 genomes]
rs7309789	1.00[AMR][1000 genomes]
rs7312269	1.00[AMR][1000 genomes]
rs73297927	1.00[AMR][1000 genomes]
rs73297940	1.00[AMR][1000 genomes]
rs73297966	1.00[AMR][1000 genomes]
rs73298000	1.00[AMR][1000 genomes]
rs73300041	1.00[AMR][1000 genomes]
rs73308073	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73308091	1.00[AMR][1000 genomes]
rs73308094	1.00[AMR][1000 genomes]
rs73308096	1.00[AMR][1000 genomes]
rs73310009	1.00[AMR][1000 genomes]
rs73310019	1.00[AMR][1000 genomes]
rs73310024	1.00[AMR][1000 genomes]
rs73311230	1.00[AMR][1000 genomes]
rs73311252	1.00[AMR][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	esv3414501	chr12:51174503-51534707	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 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	chr12:51303000-51306600	ZNF genes & repeats	hESC Derived CD184+ Endoderm 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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