Variant report

Variant	rs7777766
Chromosome Location	chr7:38101457-38101458
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs12666817	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12668164	0.89[EUR][1000 genomes]
rs12672796	0.87[EUR][1000 genomes]
rs1524072	0.94[CEU][hapmap];0.85[JPT][hapmap];0.87[EUR][1000 genomes]
rs1524074	0.94[CEU][hapmap];0.85[JPT][hapmap];0.87[EUR][1000 genomes]
rs1524075	0.94[CEU][hapmap];0.87[EUR][1000 genomes]
rs17171266	0.87[EUR][1000 genomes]
rs34247895	0.87[EUR][1000 genomes]
rs34552546	0.87[EUR][1000 genomes]
rs34719447	0.87[EUR][1000 genomes]
rs55896610	0.87[EUR][1000 genomes]
rs58100365	0.89[EUR][1000 genomes]
rs60403038	0.82[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs73126894	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7779563	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7781364	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7782762	0.82[AFR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8074	chr7:37865340-38210087	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv606624	chr7:38067723-38123667	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv887962	chr7:38093233-38203341	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	2 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	chr7:38100400-38102000	Weak transcription	Psoas Muscle	Psoas

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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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