Variant report

Variant	rs7109522
Chromosome Location	chr11:102511675-102511676
allele	G/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:19)

rs_ID	r²[population]
rs10160697	0.90[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs10160700	0.91[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs10160727	0.91[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs10895328	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11225349	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11225358	0.91[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs11225359	0.90[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs11225360	0.81[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs1940477	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28380155	0.81[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs4754860	0.83[EUR][1000 genomes]
rs4754861	0.81[EUR][1000 genomes]
rs4754862	0.83[EUR][1000 genomes]
rs7109663	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7109815	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7109950	0.91[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs7129777	0.91[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs7129790	0.91[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs7927404	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832252	chr11:102445479-102627879	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1037454	chr11:102487521-102601233	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv541156	chr11:102487521-102601233	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102508400-102511800	Weak transcription	Pancreas	Pancrea
2	chr11:102509800-102512200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr11:102510600-102512000	Enhancers	A549	lung
4	chr11:102511000-102514600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr11:102511400-102511800	Enhancers	Brain Anterior Caudate	brain
6	chr11:102511600-102511800	Enhancers	Liver	Liver
7	chr11:102511600-102512000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr11:102511600-102512200	Enhancers	Fetal Intestine Large	intestine
9	chr11:102511600-102512200	Flanking Active TSS	HepG2	liver

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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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