Variant report

Variant	rs73478367
Chromosome Location	chr6:85826472-85826473
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs58104511	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58523143	1.00[AMR][1000 genomes]
rs60352764	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60492136	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61502858	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6908734	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73478378	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73478383	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73478385	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73478393	1.00[AMR][1000 genomes]
rs73478396	1.00[AMR][1000 genomes]
rs73478401	1.00[AMR][1000 genomes]
rs73480208	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73480215	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73482302	1.00[AMR][1000 genomes]
rs73486242	1.00[AMR][1000 genomes]
rs73492352	1.00[AMR][1000 genomes]
rs7744732	1.00[AMR][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	nsv1017418	chr6:85344786-86259540	Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv538347	chr6:85344786-86259540	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv520873	chr6:85824323-85834204	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:85824400-85826800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr6:85825400-85826600	Enhancers	Fetal Lung	lung
3	chr6:85825800-85828000	Weak transcription	Fetal Muscle Leg	muscle

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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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