Variant report

Variant	rs4448664
Chromosome Location	chr11:107548826-107548827
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10789631	0.81[AFR][1000 genomes]
rs10789632	0.85[AFR][1000 genomes]
rs1545826	0.95[CHB][hapmap];0.85[JPT][hapmap];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1680251	0.85[ASN][1000 genomes]
rs1790139	0.88[ASN][1000 genomes]
rs1790140	0.88[ASN][1000 genomes]
rs2508900	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2509193	1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2509195	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28716708	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4375415	0.85[AFR][1000 genomes]
rs474459	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs474480	1.00[CHB][hapmap];0.88[JPT][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4754241	0.85[AFR][1000 genomes]
rs475875	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs477835	1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs482353	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs486531	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs490626	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs493770	1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs498880	0.84[CHB][hapmap];0.82[ASN][1000 genomes]
rs521030	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs524611	1.00[CHB][hapmap];0.85[JPT][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs525584	1.00[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs526291	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs526626	1.00[CHB][hapmap];0.85[JPT][hapmap];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs527167	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs527296	0.85[CHB][hapmap];0.80[ASN][1000 genomes]
rs531608	0.90[CHB][hapmap];0.83[ASN][1000 genomes]
rs550104	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs550514	0.95[CHB][hapmap];0.85[JPT][hapmap];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs552215	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs559126	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs561617	0.95[CHB][hapmap];0.85[ASN][1000 genomes]
rs591697	0.88[ASN][1000 genomes]
rs595138	0.85[ASN][1000 genomes]
rs599271	0.85[ASN][1000 genomes]
rs60752013	0.83[ASN][1000 genomes]
rs607867	0.98[ASN][1000 genomes]
rs612205	0.89[CHB][hapmap];0.85[JPT][hapmap];0.80[YRI][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs627021	0.90[CHB][hapmap];0.85[ASN][1000 genomes]
rs647756	1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[YRI][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs654783	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs655594	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs661269	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs665357	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs669035	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs677782	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs679748	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs694990	0.90[CHB][hapmap];0.87[ASN][1000 genomes]
rs7104429	0.84[AFR][1000 genomes]
rs73557781	0.83[ASN][1000 genomes]
rs7947474	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038368	chr11:107116577-107664181	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv541163	chr11:107116577-107664181	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv533794	chr11:107349817-108093259	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv1039425	chr11:107468681-107895836	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv427899	chr11:107471544-107805894	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
6	nsv468866	chr11:107472733-107566585	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv556377	chr11:107472733-107566585	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	esv2422201	chr11:107479362-107555825	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1052198	chr11:107509918-107684371	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
10	nsv1049524	chr11:107540937-107954011	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107547200-107550400	Enhancers	Fetal Brain Male	brain
2	chr11:107547800-107549000	Weak transcription	Fetal Brain Female	brain
3	chr11:107548600-107550400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr11:107548800-107550000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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