Variant report

Variant	rs12276405
Chromosome Location	chr11:84509954-84509955
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10501570	1.00[JPT][hapmap]
rs10501571	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10501572	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs10792782	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs10898296	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10898299	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11234157	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11234167	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs11234170	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11234171	1.00[ASN][1000 genomes]
rs11234176	1.00[ASN][1000 genomes]
rs11234178	1.00[ASN][1000 genomes]
rs11234179	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11234180	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11234181	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11234182	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11234194	0.80[CEU][hapmap]
rs11518753	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11518754	1.00[ASN][1000 genomes]
rs12271903	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12274130	1.00[CHB][hapmap]
rs12291798	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12361278	1.00[ASN][1000 genomes]
rs12361279	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12362064	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17735188	1.00[CHB][hapmap]
rs17741047	0.93[ASN][1000 genomes]
rs17741065	0.93[ASN][1000 genomes]
rs17741077	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17808095	1.00[JPT][hapmap]
rs17808225	1.00[JPT][hapmap]
rs17808315	0.93[ASN][1000 genomes]
rs1940098	1.00[JPT][hapmap]
rs1943524	1.00[ASN][1000 genomes]
rs1943691	0.84[CEU][hapmap];0.86[EUR][1000 genomes]
rs1943693	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs1943696	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1943698	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1943699	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs1943703	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1943705	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1943708	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2187359	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4367967	1.00[CHB][hapmap]
rs6592199	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6592201	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7103862	0.82[EUR][1000 genomes]
rs7107842	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7129466	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs72945887	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948410	chr11:83918339-84812001	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1045974	chr11:84187214-84708462	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1049964	chr11:84315563-84578721	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv555615	chr11:84334144-84541403	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1043987	chr11:84355133-84516193	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv541108	chr11:84355133-84516193	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1051456	chr11:84355133-84544954	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1048051	chr11:84419442-84784233	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv541109	chr11:84419442-84784233	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv898036	chr11:84420132-84576644	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv527928	chr11:84449507-84548547	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	nsv898039	chr11:84449873-84521977	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	esv2752810	chr11:84473427-84511666	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
14	nsv870278	chr11:84477088-84534255	Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
15	nsv817205	chr11:84497319-84628963	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84506400-84511800	Weak transcription	Fetal Heart	heart
2	chr11:84506600-84510000	Weak transcription	Fetal Stomach	stomach
3	chr11:84509600-84510600	Enhancers	Fetal Muscle Leg	muscle
4	chr11:84509800-84510200	Enhancers	Fetal Muscle Trunk	muscle

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