Variant report

Variant	rs56161495
Chromosome Location	chr1:56028679-56028680
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs17416725	0.84[EUR][1000 genomes]
rs17417072	0.84[EUR][1000 genomes]
rs41297891	0.84[EUR][1000 genomes]
rs41297893	0.84[EUR][1000 genomes]
rs55718597	1.00[EUR][1000 genomes]
rs55736946	1.00[EUR][1000 genomes]
rs56058312	0.92[EUR][1000 genomes]
rs56237538	1.00[EUR][1000 genomes]
rs56246158	1.00[EUR][1000 genomes]
rs57193275	1.00[EUR][1000 genomes]
rs57832473	1.00[EUR][1000 genomes]
rs61574505	1.00[EUR][1000 genomes]
rs72667829	1.00[EUR][1000 genomes]
rs72667830	1.00[EUR][1000 genomes]
rs72667831	1.00[EUR][1000 genomes]
rs72667834	1.00[EUR][1000 genomes]
rs72667835	1.00[EUR][1000 genomes]
rs72667840	1.00[EUR][1000 genomes]
rs72667842	1.00[EUR][1000 genomes]
rs72667844	1.00[EUR][1000 genomes]
rs72667851	1.00[EUR][1000 genomes]
rs72667861	0.92[EUR][1000 genomes]
rs72667865	0.92[EUR][1000 genomes]
rs72667866	0.92[EUR][1000 genomes]
rs72667868	0.92[EUR][1000 genomes]
rs72667875	0.92[EUR][1000 genomes]
rs72667878	0.84[EUR][1000 genomes]
rs72667893	0.92[EUR][1000 genomes]
rs72669719	0.84[EUR][1000 genomes]
rs72669723	0.84[EUR][1000 genomes]
rs72669726	0.84[EUR][1000 genomes]
rs72669728	0.84[EUR][1000 genomes]
rs72669729	0.84[EUR][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	nsv10184	chr1:55728755-56084833	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr1:56025800-56038400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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