Variant report

Variant	rs12335273
Chromosome Location	chr8:127676440-127676441
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10113420	0.83[EUR][1000 genomes]
rs11782631	0.91[EUR][1000 genomes]
rs13280151	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28478885	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs28669058	0.90[EUR][1000 genomes]
rs34512701	0.86[AMR][1000 genomes]
rs4416795	0.97[EUR][1000 genomes]
rs7813757	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7814010	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7827614	0.93[AMR][1000 genomes];0.97[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	nsv917354	chr8:127545903-127728374	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv891438	chr8:127670339-127845702	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr8:127613200-127686800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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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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