Variant report

Variant	rs275596
Chromosome Location	chr11:45610959-45610960
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1013700	0.93[ASN][1000 genomes]
rs10838489	0.97[ASN][1000 genomes]
rs1107449	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1158404	0.82[ASN][1000 genomes]
rs1488682	0.97[ASN][1000 genomes]
rs1488683	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1488684	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1868098	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2166748	0.95[ASN][1000 genomes]
rs7127267	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs728516	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7396878	0.80[AFR][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	nsv897310	chr11:45487041-45631953	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	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	chr11:45608200-45611800	Weak transcription	Fetal Brain Male	brain
2	chr11:45609000-45611200	Weak transcription	Brain Germinal Matrix	brain
3	chr11:45609400-45614000	Weak transcription	Fetal Brain Female	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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