Variant report

Variant	rs11926348
Chromosome Location	chr3:89865988-89865989
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs11923167	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11925483	0.88[AFR][1000 genomes]
rs11926549	0.94[AFR][1000 genomes]
rs11927661	0.94[AFR][1000 genomes]
rs11928160	0.89[AFR][1000 genomes]
rs11928161	0.89[AFR][1000 genomes]
rs11928197	0.94[AFR][1000 genomes]
rs11929614	0.86[AFR][1000 genomes]
rs11929622	0.92[AFR][1000 genomes]
rs11929639	0.92[AFR][1000 genomes]
rs1357168	0.90[AFR][1000 genomes]
rs1915735	0.91[AFR][1000 genomes]
rs28831116	1.00[AMR][1000 genomes]
rs34684257	0.91[AFR][1000 genomes]
rs55743058	0.94[AFR][1000 genomes]
rs55900084	0.91[AFR][1000 genomes]
rs56089352	0.90[AFR][1000 genomes]
rs56108378	0.91[AFR][1000 genomes]
rs56763170	0.94[AFR][1000 genomes]
rs56978342	0.94[AFR][1000 genomes]
rs57243284	0.90[AFR][1000 genomes]
rs57601270	0.86[AFR][1000 genomes]
rs57803709	0.82[AFR][1000 genomes]
rs58016519	0.80[AFR][1000 genomes]
rs59015121	0.91[AFR][1000 genomes]
rs59399871	0.94[AFR][1000 genomes]
rs60329202	0.91[AFR][1000 genomes]
rs60507817	0.97[AFR][1000 genomes]
rs60621365	1.00[AFR][1000 genomes]
rs61425643	1.00[AMR][1000 genomes]
rs6551424	1.00[AMR][1000 genomes]
rs6551442	0.94[AFR][1000 genomes]
rs6551443	0.94[AFR][1000 genomes]
rs6774114	0.94[AFR][1000 genomes]
rs6774428	0.86[AFR][1000 genomes]
rs6776405	0.94[AFR][1000 genomes]
rs6789090	0.97[AFR][1000 genomes]
rs6798157	0.88[AFR][1000 genomes]
rs6807535	0.94[AFR][1000 genomes]
rs6807901	0.94[AFR][1000 genomes]
rs72914021	1.00[AMR][1000 genomes]
rs72914023	0.85[AFR][1000 genomes]
rs72914070	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72915828	0.97[AFR][1000 genomes]
rs72915834	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72915835	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72915840	0.94[AFR][1000 genomes]
rs72915842	0.94[AFR][1000 genomes]
rs72915844	0.94[AFR][1000 genomes]
rs72917606	0.87[AFR][1000 genomes]
rs72917631	0.91[AFR][1000 genomes]
rs72917640	0.91[AFR][1000 genomes]
rs72917652	0.91[AFR][1000 genomes]
rs72917689	0.94[AFR][1000 genomes]
rs72925673	1.00[AMR][1000 genomes]
rs72929651	1.00[AMR][1000 genomes]
rs7610460	0.92[AFR][1000 genomes]
rs7628770	0.94[AFR][1000 genomes]
rs7653528	0.94[AFR][1000 genomes]
rs9682231	1.00[AFR][1000 genomes]
rs9683254	1.00[AFR][1000 genomes]
rs9714298	0.91[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008018	chr3:89382031-90254063	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv536639	chr3:89382031-90254063	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1010932	chr3:89424428-90192503	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1010021	chr3:89521983-90141988	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv530024	chr3:89548440-90304841	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv869889	chr3:89653238-90087372	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1013502	chr3:89670525-89915342	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv536641	chr3:89670525-89915342	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv834761	chr3:89718508-89877335	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv1005444	chr3:89803641-90030755	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1008130	chr3:89837442-90192503	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr3:89860400-89867000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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