Variant report

Variant	rs73869119
Chromosome Location	chr3:150770388-150770389
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs16863137	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56121010	0.86[AFR][1000 genomes]
rs56218140	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57319865	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57881928	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61112399	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6786527	1.00[EUR][1000 genomes]
rs73011152	1.00[EUR][1000 genomes]
rs73011164	1.00[EUR][1000 genomes]
rs73011173	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73012964	0.84[AFR][1000 genomes]
rs73869114	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7629984	0.85[AMR][1000 genomes];1.00[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	nsv915879	chr3:150607390-150860207	Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv829756	chr3:150692636-150889738	Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr3:150769400-150771000	Enhancers	Liver	Liver
2	chr3:150769600-150772000	Enhancers	Fetal Intestine Small	intestine
3	chr3:150770000-150770800	Enhancers	Fetal Intestine Large	intestine

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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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