Variant report

Variant	rs55901470
Chromosome Location	chr6:72269868-72269869
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs16881389	1.00[AMR][1000 genomes]
rs199628	1.00[AMR][1000 genomes]
rs56062820	1.00[AMR][1000 genomes]
rs562111	1.00[AMR][1000 genomes]
rs56280910	1.00[AMR][1000 genomes]
rs57603244	1.00[AMR][1000 genomes]
rs58186674	1.00[AMR][1000 genomes]
rs61425931	1.00[AMR][1000 genomes]
rs73747149	1.00[AMR][1000 genomes]
rs73747151	1.00[AMR][1000 genomes]
rs73747152	1.00[AMR][1000 genomes]
rs73747154	1.00[AMR][1000 genomes]
rs73747156	1.00[AMR][1000 genomes]
rs73747159	1.00[AMR][1000 genomes]
rs73747160	1.00[AMR][1000 genomes]
rs73747161	1.00[AMR][1000 genomes]
rs73747174	1.00[AMR][1000 genomes]
rs73747175	1.00[AMR][1000 genomes]
rs73747176	1.00[AMR][1000 genomes]
rs73747177	1.00[AMR][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	nsv830684	chr6:72094842-72282684	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	488 gene(s)	inside rSNPs	diseases
2	nsv830685	chr6:72244007-72410757	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr6:72269800-72270400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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