Variant report

Variant	rs2200497
Chromosome Location	chr11:49272206-49272207
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10734597	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10742937	0.89[ASN][1000 genomes]
rs10769571	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10769573	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10839248	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10839251	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10839252	0.83[ASN][1000 genomes]
rs10839253	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10839254	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10839255	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10839257	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10839259	0.86[ASN][1000 genomes]
rs11040289	0.82[ASN][1000 genomes]
rs11040311	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11040322	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11822117	0.96[ASN][1000 genomes]
rs11823826	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11827867	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12221758	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1851981	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1872610	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2005014	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs202681	0.81[ASN][1000 genomes]
rs202695	0.80[ASN][1000 genomes]
rs202696	0.80[ASN][1000 genomes]
rs202698	0.81[ASN][1000 genomes]
rs202701	0.80[ASN][1000 genomes]
rs2866347	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2903253	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2931177	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs3881244	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3881245	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4088771	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4303234	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4373925	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs596754	0.90[ASN][1000 genomes]
rs597683	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs600974	0.90[ASN][1000 genomes]
rs611931	0.90[ASN][1000 genomes]
rs613429	0.84[ASN][1000 genomes]
rs613450	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs628194	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs636059	0.90[ASN][1000 genomes]
rs6485971	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs650826	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs651278	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7101591	0.84[ASN][1000 genomes]
rs7103267	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7103270	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7106905	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7111262	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7114817	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7115507	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7117025	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7118094	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7118378	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7118379	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7121968	0.96[ASN][1000 genomes]
rs7122073	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7125691	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7131181	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7131190	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7131572	0.84[ASN][1000 genomes]
rs7481212	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7925859	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7935256	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7951210	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv469956	chr11:48922645-49862647	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv554347	chr11:49111467-49862647	Enhancers Active TSS Strong transcription Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1044070	chr11:49147743-49448774	Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv525454	chr11:49156039-49570587	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv518571	chr11:49162948-49627833	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv2758269	chr11:49212237-49468966	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	esv2759825	chr11:49212237-49468966	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv972016	chr11:49246163-49330536	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:49272200-49272600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr11:49272200-49272600	Enhancers	HUES48 Cell Line	embryonic stem cell

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