Variant report

Variant	rs10201376
Chromosome Location	chr2:123843276-123843277
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10187181	0.94[EUR][1000 genomes]
rs10192812	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs10203326	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10210632	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12373639	0.94[EUR][1000 genomes]
rs1399642	0.94[EUR][1000 genomes]
rs1399643	0.94[EUR][1000 genomes]
rs17009319	0.94[EUR][1000 genomes]
rs17009364	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs2419072	0.94[EUR][1000 genomes]
rs2661033	0.94[EUR][1000 genomes]
rs2661037	0.94[EUR][1000 genomes]
rs2661038	0.94[EUR][1000 genomes]
rs2661039	0.94[EUR][1000 genomes]
rs2661040	0.94[EUR][1000 genomes]
rs2673186	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs72964558	0.94[EUR][1000 genomes]
rs908272	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492280	chr2:123447662-123973577	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2760647	chr2:123678437-124619697	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1010200	chr2:123816326-123887210	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv524501	chr2:123840759-123849482	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:123839400-123844200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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