Variant report

Variant	rs11234648
Chromosome Location	chr11:86133937-86133938
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10466700	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10466729	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10466730	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11234643	0.85[LWK][hapmap];0.82[MKK][hapmap];0.84[YRI][hapmap];0.83[AFR][1000 genomes]
rs11234647	1.00[CEU][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11824889	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11825033	0.82[CEU][hapmap];0.82[EUR][1000 genomes]
rs11826066	1.00[MEX][hapmap];0.88[TSI][hapmap]
rs11828146	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11828283	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12269969	0.82[EUR][1000 genomes]
rs12270471	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12270570	0.92[AFR][1000 genomes]
rs12270761	1.00[ASN][1000 genomes]
rs12270790	1.00[JPT][hapmap];0.90[YRI][hapmap];0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12272259	0.83[ASN][1000 genomes]
rs12272318	0.85[AFR][1000 genomes]
rs12276248	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12277432	1.00[ASN][1000 genomes]
rs12278188	0.85[CEU][hapmap]
rs12278247	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12280555	0.87[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12280833	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12281645	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12283035	1.00[ASN][1000 genomes]
rs12285249	1.00[JPT][hapmap];0.90[YRI][hapmap];1.00[ASN][1000 genomes]
rs12288560	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12289817	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12291532	1.00[ASN][1000 genomes]
rs12292316	1.00[CEU][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.87[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12293159	1.00[ASN][1000 genomes]
rs12293545	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12294756	1.00[ASN][1000 genomes]
rs12804130	1.00[ASN][1000 genomes]
rs12804407	1.00[ASN][1000 genomes]
rs12805940	0.85[JPT][hapmap];1.00[ASN][1000 genomes]
rs1452136	1.00[ASN][1000 genomes]
rs1452137	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1458381	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17149063	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17149064	1.00[JPT][hapmap];0.95[YRI][hapmap];0.91[AFR][1000 genomes]
rs17819176	0.85[JPT][hapmap];1.00[ASN][1000 genomes]
rs2242142	1.00[JPT][hapmap];0.90[YRI][hapmap];1.00[ASN][1000 genomes]
rs2279047	0.85[JPT][hapmap];1.00[ASN][1000 genomes]
rs34416639	1.00[ASN][1000 genomes]
rs34939684	1.00[ASN][1000 genomes]
rs35686713	1.00[ASN][1000 genomes]
rs3741001	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3741002	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3741003	1.00[CEU][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3781806	1.00[ASN][1000 genomes]
rs3781813	1.00[ASN][1000 genomes]
rs3824953	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs56009909	1.00[ASN][1000 genomes]
rs58228993	1.00[ASN][1000 genomes]
rs58354189	1.00[ASN][1000 genomes]
rs66833360	1.00[ASN][1000 genomes]
rs66872826	1.00[ASN][1000 genomes]
rs7107941	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7108053	0.85[JPT][hapmap]
rs7122296	1.00[JPT][hapmap];0.90[YRI][hapmap];1.00[ASN][1000 genomes]
rs7122406	1.00[JPT][hapmap];0.91[LWK][hapmap];0.98[MKK][hapmap];0.90[YRI][hapmap];1.00[ASN][1000 genomes]
rs7129977	1.00[ASN][1000 genomes]
rs72953614	1.00[ASN][1000 genomes]
rs7932664	1.00[JPT][hapmap];0.91[LWK][hapmap];0.97[MKK][hapmap];0.94[YRI][hapmap];0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7936577	0.85[CEU][hapmap]
rs7948566	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7948764	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044081	chr11:86133641-86868560	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv541118	chr11:86133641-86868560	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86106600-86134600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:86108600-86138600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr11:86117800-86142200	Weak transcription	Fetal Stomach	stomach
4	chr11:86118200-86151000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr11:86118400-86142800	Weak transcription	Left Ventricle	heart
6	chr11:86119400-86135000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr11:86119600-86142200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr11:86123600-86136800	Weak transcription	Brain Hippocampus Middle	brain
9	chr11:86124600-86142200	Weak transcription	Aorta	Aorta
10	chr11:86124800-86136600	Weak transcription	Brain Anterior Caudate	brain
11	chr11:86130400-86134600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr11:86131400-86142400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr11:86131600-86136000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:86132200-86142200	Weak transcription	Spleen	Spleen
15	chr11:86132600-86134600	Weak transcription	Fetal Lung	lung
16	chr11:86132800-86135000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr11:86133000-86135400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr11:86133200-86134600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr11:86133200-86134800	Enhancers	Placenta	Placenta
20	chr11:86133200-86135200	Enhancers	Fetal Intestine Large	intestine
21	chr11:86133200-86135400	Enhancers	K562	blood
22	chr11:86133400-86134800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr11:86133600-86134000	Weak transcription	Ovary	ovary
24	chr11:86133600-86134600	Enhancers	Fetal Intestine Small	intestine

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