Variant report

Variant	rs2335377
Chromosome Location	chr1:196155266-196155267
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10754183	0.82[ASN][1000 genomes]
rs10801521	0.83[ASN][1000 genomes]
rs10922047	0.83[ASN][1000 genomes]
rs1325303	0.83[ASN][1000 genomes]
rs1325304	0.83[ASN][1000 genomes]
rs1325305	0.80[ASN][1000 genomes]
rs1325307	0.83[ASN][1000 genomes]
rs1886628	0.83[ASN][1000 genomes]
rs1886629	0.83[ASN][1000 genomes]
rs1886630	0.83[ASN][1000 genomes]
rs1925325	0.85[ASN][1000 genomes]
rs1925326	0.83[ASN][1000 genomes]
rs2094026	0.83[ASN][1000 genomes]
rs2094027	0.83[ASN][1000 genomes]
rs2104405	0.83[ASN][1000 genomes]
rs2335376	0.80[ASN][1000 genomes]
rs2335378	0.83[ASN][1000 genomes]
rs2335379	0.83[ASN][1000 genomes]
rs2335380	0.83[ASN][1000 genomes]
rs2335382	0.83[ASN][1000 genomes]
rs2335383	0.83[ASN][1000 genomes]
rs2335384	0.83[ASN][1000 genomes]
rs2878402	0.83[ASN][1000 genomes]
rs4364854	0.87[ASN][1000 genomes]
rs4474231	0.82[ASN][1000 genomes]
rs4474232	0.83[ASN][1000 genomes]
rs6658670	0.83[ASN][1000 genomes]
rs6658892	0.83[ASN][1000 genomes]
rs6661581	0.80[ASN][1000 genomes]
rs6667493	0.83[ASN][1000 genomes]
rs6680145	0.83[ASN][1000 genomes]
rs6684402	0.83[ASN][1000 genomes]
rs6690380	0.80[ASN][1000 genomes]
rs6692987	0.80[ASN][1000 genomes]
rs72750530	0.80[ASN][1000 genomes]
rs7511738	0.83[ASN][1000 genomes]
rs7514160	0.83[ASN][1000 genomes]
rs7514163	0.83[ASN][1000 genomes]
rs7514363	0.83[ASN][1000 genomes]
rs7515038	0.80[ASN][1000 genomes]
rs912761	0.83[ASN][1000 genomes]
rs912763	0.83[ASN][1000 genomes]
rs927724	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872948	chr1:195872295-196236425	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv470769	chr1:195901676-196187665	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv534209	chr1:196011881-196208885	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv872951	chr1:196027872-196166278	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv1836908	chr1:196142986-196177193	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:196151400-196163200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr1:196151600-196155800	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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