Variant report

Variant	rs73451196
Chromosome Location	chr6:55423149-55423150
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11961070	1.00[AMR][1000 genomes]
rs3885995	0.87[AFR][1000 genomes]
rs55993267	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57555928	1.00[AMR][1000 genomes]
rs58006571	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58660660	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59077790	1.00[AMR][1000 genomes]
rs59493948	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73449066	1.00[AMR][1000 genomes]
rs73449078	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73449086	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451113	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451178	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73451193	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73744632	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73744633	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73746355	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034037	chr6:55222409-56069600	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv948358	chr6:55351282-55477277	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1026411	chr6:55372845-55653498	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55419600-55433600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr6:55422400-55423400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:55422600-55433400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:55423000-55424000	Weak transcription	Fetal Heart	heart
5	chr6:55423000-55425200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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