Variant report

Variant	rs6766954
Chromosome Location	chr3:135217331-135217332
allele	A/G
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:18)

rs_ID	r²[population]
rs10935169	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11915681	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11915808	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12486878	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12488558	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12497034	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17187040	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17246571	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17246773	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs55887730	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs698267	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs711964	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs711966	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73229924	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73229925	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs824096	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs824284	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs863734	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460860	chr3:135107678-135769006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv591829	chr3:135107678-135769006	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:135210200-135221400	Weak transcription	Fetal Brain Male	brain
2	chr3:135210600-135222600	Weak transcription	Psoas Muscle	Psoas
3	chr3:135217200-135217400	Enhancers	Brain Hippocampus Middle	brain

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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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