Variant report

Variant	rs10265596
Chromosome Location	chr7:21047023-21047024
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10229329	0.90[EUR][1000 genomes]
rs10231756	0.98[EUR][1000 genomes]
rs10240922	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10246458	0.90[EUR][1000 genomes]
rs10263153	0.90[EUR][1000 genomes]
rs10270424	0.95[EUR][1000 genomes]
rs10275186	0.90[EUR][1000 genomes]
rs10499520	0.98[EUR][1000 genomes]
rs11766574	0.90[EUR][1000 genomes]
rs11769317	0.91[EUR][1000 genomes]
rs11773336	0.95[EUR][1000 genomes]
rs12532948	0.98[EUR][1000 genomes]
rs12533676	0.95[EUR][1000 genomes]
rs12668632	0.97[EUR][1000 genomes]
rs13221970	0.97[EUR][1000 genomes]
rs13246880	0.97[EUR][1000 genomes]
rs13340545	0.98[EUR][1000 genomes]
rs2215677	0.80[EUR][1000 genomes]
rs2390411	0.95[EUR][1000 genomes]
rs41304921	0.90[EUR][1000 genomes]
rs4365987	0.90[EUR][1000 genomes]
rs73263890	0.90[EUR][1000 genomes]
rs73263897	0.90[EUR][1000 genomes]
rs73268090	0.91[EUR][1000 genomes]
rs73269804	0.98[EUR][1000 genomes]
rs7784357	0.90[EUR][1000 genomes]
rs7798796	0.87[EUR][1000 genomes]
rs7811627	0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030726	chr7:20506095-21086719	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv830920	chr7:21014535-21201580	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv3478244	chr7:21044211-21417347	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3478245	chr7:21044211-21417347	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:21046800-21047600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:21047000-21047200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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