Variant report

Variant	rs61918530
Chromosome Location	chr11:93364502-93364503
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10047479	1.00[EUR][1000 genomes]
rs10047481	1.00[EUR][1000 genomes]
rs10047484	1.00[EUR][1000 genomes]
rs1011008	1.00[EUR][1000 genomes]
rs10128669	1.00[EUR][1000 genomes]
rs10128725	1.00[EUR][1000 genomes]
rs10128726	1.00[EUR][1000 genomes]
rs11020438	1.00[EUR][1000 genomes]
rs11020448	1.00[EUR][1000 genomes]
rs11020467	1.00[EUR][1000 genomes]
rs11020468	1.00[EUR][1000 genomes]
rs11020469	1.00[EUR][1000 genomes]
rs11822965	1.00[EUR][1000 genomes]
rs11828991	1.00[EUR][1000 genomes]
rs12271543	1.00[EUR][1000 genomes]
rs12274112	1.00[EUR][1000 genomes]
rs12276266	1.00[EUR][1000 genomes]
rs12278092	1.00[EUR][1000 genomes]
rs12278291	1.00[EUR][1000 genomes]
rs12279634	1.00[EUR][1000 genomes]
rs12279657	1.00[EUR][1000 genomes]
rs12283126	1.00[EUR][1000 genomes]
rs12284176	1.00[EUR][1000 genomes]
rs12291408	1.00[EUR][1000 genomes]
rs12293939	1.00[EUR][1000 genomes]
rs13377252	1.00[EUR][1000 genomes]
rs13377541	1.00[EUR][1000 genomes]
rs16919124	1.00[EUR][1000 genomes]
rs56705833	1.00[EUR][1000 genomes]
rs58111338	1.00[EUR][1000 genomes]
rs60224981	1.00[EUR][1000 genomes]
rs60410024	1.00[EUR][1000 genomes]
rs61904920	1.00[EUR][1000 genomes]
rs61904941	1.00[EUR][1000 genomes]
rs61904958	1.00[EUR][1000 genomes]
rs61918547	1.00[EUR][1000 genomes]
rs61918549	1.00[EUR][1000 genomes]
rs61918550	1.00[EUR][1000 genomes]
rs61918551	1.00[EUR][1000 genomes]
rs61918553	1.00[EUR][1000 genomes]
rs61918554	1.00[EUR][1000 genomes]
rs61918557	1.00[EUR][1000 genomes]
rs61921277	1.00[EUR][1000 genomes]
rs674150	1.00[EUR][1000 genomes]
rs7109215	1.00[EUR][1000 genomes]
rs7111581	1.00[EUR][1000 genomes]
rs7113200	1.00[EUR][1000 genomes]
rs7128116	1.00[EUR][1000 genomes]
rs7130267	1.00[EUR][1000 genomes]
rs7930519	1.00[EUR][1000 genomes]
rs7952443	1.00[EUR][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	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
2	nsv975401	chr11:93364502-93390549	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	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	chr11:93356600-93364600	Weak transcription	Pancreas	Pancrea

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