Variant report

Variant	rs1869912
Chromosome Location	chr11:93186433-93186434
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10831053	1.00[ASN][1000 genomes]
rs11020389	1.00[ASN][1000 genomes]
rs11020403	1.00[ASN][1000 genomes]
rs11820614	1.00[ASN][1000 genomes]
rs2045313	1.00[ASN][1000 genomes]
rs2045461	1.00[ASN][1000 genomes]
rs2045462	1.00[ASN][1000 genomes]
rs2198797	1.00[ASN][1000 genomes]
rs2605591	1.00[ASN][1000 genomes]
rs2605592	1.00[ASN][1000 genomes]
rs2605594	1.00[ASN][1000 genomes]
rs2605595	1.00[ASN][1000 genomes]
rs2605598	1.00[ASN][1000 genomes]
rs2605599	1.00[ASN][1000 genomes]
rs2605601	1.00[ASN][1000 genomes]
rs2605602	1.00[ASN][1000 genomes]
rs2605605	1.00[ASN][1000 genomes]
rs2608273	1.00[ASN][1000 genomes]
rs2608277	1.00[ASN][1000 genomes]
rs2608278	1.00[ASN][1000 genomes]
rs2658794	1.00[ASN][1000 genomes]
rs2658795	1.00[ASN][1000 genomes]
rs2658796	1.00[ASN][1000 genomes]
rs2658800	1.00[ASN][1000 genomes]
rs2658802	1.00[ASN][1000 genomes]
rs6483246	1.00[ASN][1000 genomes]
rs7114771	1.00[ASN][1000 genomes]
rs7124358	1.00[ASN][1000 genomes]
rs897556	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	nsv1039134	chr11:92790000-93219942	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv898181	chr11:93072843-93662459	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
3	nsv1039623	chr11:93141461-93328739	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	esv2760208	chr11:93172673-93266594	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	3 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	chr11:93183600-93191400	Weak transcription	Pancreas	Pancrea

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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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