Variant report

Variant	rs58307895
Chromosome Location	chr6:150291976-150291977
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs3860813	1.00[AMR][1000 genomes]
rs55650377	1.00[AMR][1000 genomes]
rs56706316	1.00[AMR][1000 genomes]
rs56896927	1.00[AMR][1000 genomes]
rs57472228	1.00[AMR][1000 genomes]
rs58763378	1.00[AMR][1000 genomes]
rs58946697	1.00[AMR][1000 genomes]
rs59281875	1.00[AMR][1000 genomes]
rs59602990	1.00[AMR][1000 genomes]
rs59878448	1.00[AMR][1000 genomes]
rs60248818	1.00[AMR][1000 genomes]
rs60386924	1.00[AMR][1000 genomes]
rs60494754	1.00[AMR][1000 genomes]
rs60897658	1.00[AMR][1000 genomes]
rs61084626	1.00[AMR][1000 genomes]
rs61230059	1.00[AMR][1000 genomes]
rs61285074	1.00[AMR][1000 genomes]
rs73612461	1.00[AMR][1000 genomes]
rs73612479	1.00[AMR][1000 genomes]
rs7748726	1.00[AMR][1000 genomes]
rs877114	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	nsv886764	chr6:150114745-150393683	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv517022	chr6:150145001-150426272	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv970175	chr6:150286661-150300237	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 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	chr6:150286800-150294800	Weak transcription	HSMMtube	muscle
2	chr6:150288600-150295600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr6:150291600-150292200	Weak transcription	Spleen	Spleen

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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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