Variant report

Variant	rs12805464
Chromosome Location	chr11:83732592-83732593
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 125 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:115)

rs_ID	r²[population]
rs11233848	1.00[JPT][hapmap]
rs11820047	1.00[TSI][hapmap]
rs12785867	1.00[AFR][1000 genomes]
rs12786173	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12786293	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12786844	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12787995	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12789072	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12789666	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12789896	0.85[TSI][hapmap]
rs12790276	1.00[MEX][hapmap];1.00[AFR][1000 genomes]
rs12791107	1.00[JPT][hapmap]
rs12791771	1.00[CEU][hapmap]
rs12791934	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12792083	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12793913	1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs12794134	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12794213	1.00[AFR][1000 genomes]
rs12795168	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12796172	1.00[AFR][1000 genomes]
rs12797177	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12797793	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12799748	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12800687	1.00[CEU][hapmap]
rs12801228	1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs12802882	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12804520	1.00[MEX][hapmap];1.00[AFR][1000 genomes]
rs12804617	1.00[MEX][hapmap]
rs12805074	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12805402	1.00[MEX][hapmap]
rs12805533	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12805593	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12805936	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12806818	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12807339	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12808113	1.00[MEX][hapmap];1.00[AFR][1000 genomes]
rs12808131	1.00[AFR][1000 genomes]
rs12808232	1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs12808867	1.00[AFR][1000 genomes]
rs12809044	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17146978	1.00[GIH][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap]
rs17561231	1.00[AFR][1000 genomes]
rs2187553	1.00[AFR][1000 genomes]
rs2449598	1.00[MEX][hapmap];1.00[AFR][1000 genomes]
rs34012933	1.00[AFR][1000 genomes]
rs34045362	1.00[AFR][1000 genomes]
rs34131208	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34133101	1.00[AFR][1000 genomes]
rs34150725	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34197413	1.00[AFR][1000 genomes]
rs34211389	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34279739	1.00[AFR][1000 genomes]
rs34281369	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34302412	1.00[AFR][1000 genomes]
rs34309181	1.00[AFR][1000 genomes]
rs34316246	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34413586	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34436974	1.00[AFR][1000 genomes]
rs34655432	1.00[AFR][1000 genomes]
rs34658258	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34716185	1.00[AFR][1000 genomes]
rs34745106	1.00[AFR][1000 genomes]
rs34747709	1.00[AFR][1000 genomes]
rs34756786	1.00[AFR][1000 genomes]
rs34826061	1.00[AFR][1000 genomes]
rs34846175	1.00[AFR][1000 genomes]
rs34899787	1.00[AFR][1000 genomes]
rs34949067	1.00[AFR][1000 genomes]
rs35240755	1.00[AFR][1000 genomes]
rs35268360	1.00[AFR][1000 genomes]
rs35275366	1.00[AFR][1000 genomes]
rs35292700	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35307147	1.00[AFR][1000 genomes]
rs35337045	1.00[AFR][1000 genomes]
rs35388672	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35494684	1.00[AFR][1000 genomes]
rs35532485	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35540097	1.00[AFR][1000 genomes]
rs35583535	1.00[AFR][1000 genomes]
rs35629749	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35693607	1.00[AFR][1000 genomes]
rs35704316	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35728121	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35804057	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35918539	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35990771	1.00[AFR][1000 genomes]
rs36034592	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs36165842	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36189811	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4133461	1.00[AFR][1000 genomes]
rs7109170	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs7115103	1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs71465566	1.00[AFR][1000 genomes]
rs71465567	1.00[AFR][1000 genomes]
rs71465568	1.00[AFR][1000 genomes]
rs71465569	1.00[AFR][1000 genomes]
rs71465573	1.00[AFR][1000 genomes]
rs71465574	1.00[AFR][1000 genomes]
rs71465575	1.00[AFR][1000 genomes]
rs71465577	1.00[AFR][1000 genomes]
rs71465579	1.00[AFR][1000 genomes]
rs71465580	1.00[AFR][1000 genomes]
rs71465581	1.00[AFR][1000 genomes]
rs71465582	1.00[AFR][1000 genomes]
rs71465583	1.00[AFR][1000 genomes]
rs71469609	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71469611	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71469615	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71469619	1.00[AFR][1000 genomes]
rs71469623	1.00[AFR][1000 genomes]
rs7482523	1.00[AFR][1000 genomes]
rs7934379	1.00[MEX][hapmap]
rs963090	1.00[MEX][hapmap];1.00[AFR][1000 genomes]
rs963091	1.00[AFR][1000 genomes]
rs963092	1.00[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	nsv898025	chr11:83658909-83796678	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
2	nsv1039924	chr11:83662904-83993497	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv541102	chr11:83662904-83993497	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv898026	chr11:83685801-83789540	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv1814410	chr11:83696133-83775326	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
6	esv1809938	chr11:83716145-83789540	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv898027	chr11:83717887-83798485	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
8	nsv898028	chr11:83717887-83817360	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
9	nsv898029	chr11:83717887-83939591	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv898030	chr11:83730570-83789540	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83728200-83733200	Enhancers	Brain Hippocampus Middle	brain
2	chr11:83730200-83733600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:83730600-83733600	Enhancers	Brain Angular Gyrus	brain
4	chr11:83730600-83734000	Enhancers	Brain Substantia Nigra	brain
5	chr11:83730600-83734400	Enhancers	Brain Cingulate Gyrus	brain
6	chr11:83731000-83734000	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr11:83731000-83734600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:83731200-83733000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr11:83731200-83734000	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr11:83731400-83732600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr11:83731400-83733200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr11:83731400-83734200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr11:83731600-83733200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr11:83731600-83733200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr11:83731600-83733600	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chr11:83731800-83733000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr11:83731800-83733000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr11:83731800-83734200	Enhancers	Colon Smooth Muscle	Colon
19	chr11:83732000-83733000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr11:83732000-83733000	Weak transcription	Ovary	ovary
21	chr11:83732000-83733400	Enhancers	Stomach Smooth Muscle	stomach
22	chr11:83732000-83734000	Enhancers	Brain Anterior Caudate	brain
23	chr11:83732200-83733200	Weak transcription	Brain Germinal Matrix	brain
24	chr11:83732200-83734400	Enhancers	Rectal Smooth Muscle	rectum
25	chr11:83732400-83733200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:83732400-83733600	Enhancers	Fetal Heart	heart
27	chr11:83732400-83734200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr11:83732400-83734400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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