Variant report

Variant	rs3018193
Chromosome Location	chr11:56943234-56943235
allele	A/C
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:18)

rs_ID	r²[population]
rs11228901	1.00[AMR][1000 genomes]
rs11501564	1.00[AMR][1000 genomes]
rs12275563	1.00[AMR][1000 genomes]
rs12275655	1.00[AMR][1000 genomes]
rs12277644	1.00[AMR][1000 genomes]
rs12288446	1.00[AMR][1000 genomes]
rs12289270	1.00[AMR][1000 genomes]
rs12290460	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12290493	1.00[AMR][1000 genomes]
rs2860248	1.00[AMR][1000 genomes]
rs2860249	1.00[AMR][1000 genomes]
rs2860311	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2860313	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2860510	1.00[AMR][1000 genomes]
rs2957193	1.00[AMR][1000 genomes]
rs2960567	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3016754	1.00[AMR][1000 genomes]
rs3017570	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	nsv915640	chr11:56814841-57139786	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv482317	chr11:56857026-57028631	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr11:56942200-56943400	Enhancers	K562	blood
2	chr11:56942200-56944800	Weak transcription	Aorta	Aorta
3	chr11:56942400-56945000	Weak transcription	Stomach Mucosa	stomach

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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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