Variant report

Variant	rs11697708
Chromosome Location	chr20:13992268-13992269
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11696504	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11697554	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1406923	1.00[ASN][1000 genomes]
rs1810689	1.00[ASN][1000 genomes]
rs1980701	1.00[ASN][1000 genomes]
rs2038674	1.00[ASN][1000 genomes]
rs2209018	1.00[ASN][1000 genomes]
rs2327819	1.00[ASN][1000 genomes]
rs3940133	1.00[ASN][1000 genomes]
rs4814289	1.00[ASN][1000 genomes]
rs4814290	1.00[ASN][1000 genomes]
rs59177302	1.00[ASN][1000 genomes]
rs6033888	1.00[ASN][1000 genomes]
rs6033897	1.00[ASN][1000 genomes]
rs6042525	1.00[ASN][1000 genomes]
rs6042548	1.00[ASN][1000 genomes]
rs6042552	1.00[ASN][1000 genomes]
rs6042553	1.00[ASN][1000 genomes]
rs6042581	1.00[ASN][1000 genomes]
rs6079309	1.00[ASN][1000 genomes]
rs6079331	1.00[ASN][1000 genomes]
rs6079346	1.00[ASN][1000 genomes]
rs6079350	1.00[ASN][1000 genomes]
rs6079353	1.00[ASN][1000 genomes]
rs6105221	1.00[ASN][1000 genomes]
rs6110194	1.00[ASN][1000 genomes]
rs7261965	1.00[ASN][1000 genomes]
rs73255018	1.00[ASN][1000 genomes]
rs73255080	1.00[ASN][1000 genomes]
rs73264804	1.00[ASN][1000 genomes]
rs73269439	1.00[ASN][1000 genomes]
rs73900790	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8118198	1.00[ASN][1000 genomes]
rs9753755	1.00[ASN][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	nsv916202	chr20:13421724-14043615	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1066810	chr20:13451869-14432454	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv912689	chr20:13570331-14155881	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv531479	chr20:13632491-14434432	Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 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	chr20:13977400-13996200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr20:13992200-13992800	ZNF genes & repeats	Fetal Intestine Small	intestine

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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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