Variant report

Variant	rs2678901
Chromosome Location	chr2:58138651-58138652
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs10188070	0.94[JPT][hapmap]
rs1040224	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1040225	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10496078	0.81[EUR][1000 genomes]
rs10496079	0.80[EUR][1000 genomes]
rs10865304	0.81[EUR][1000 genomes]
rs11898858	0.82[EUR][1000 genomes]
rs12622856	0.84[JPT][hapmap]
rs12713358	0.82[EUR][1000 genomes]
rs12713370	0.93[CEU][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs12990792	0.81[EUR][1000 genomes]
rs1356544	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1356545	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1401100	0.92[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1402398	0.83[EUR][1000 genomes]
rs1518393	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1518394	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1518395	0.92[CEU][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs1518399	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs1568252	0.84[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs1568253	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1568254	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1568450	0.83[EUR][1000 genomes]
rs1589407	0.83[EUR][1000 genomes]
rs2090793	0.83[EUR][1000 genomes]
rs2139053	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2139054	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2176546	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2312141	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2312147	0.89[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs2465804	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2678870	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2678880	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2678881	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2678889	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2678890	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2678891	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2678896	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2678897	0.89[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2678903	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2678904	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2678905	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2678906	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2678908	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2678910	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2678915	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2683614	0.83[EUR][1000 genomes]
rs2683616	0.83[EUR][1000 genomes]
rs2683619	0.83[EUR][1000 genomes]
rs2683620	0.83[EUR][1000 genomes]
rs2683628	0.83[EUR][1000 genomes]
rs2683629	0.83[EUR][1000 genomes]
rs2683634	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2717001	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2717002	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2717003	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2717004	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2717006	0.93[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2717007	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2717015	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2717018	0.83[EUR][1000 genomes]
rs2717019	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs2717023	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2717024	0.96[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap]
rs2717027	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2717031	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2717032	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2717035	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2717036	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2717040	0.92[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2717041	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2717043	0.82[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs2717048	0.83[EUR][1000 genomes]
rs2717056	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2717063	0.92[EUR][1000 genomes]
rs2717068	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2717075	0.83[EUR][1000 genomes]
rs28718871	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2953439	0.83[EUR][1000 genomes]
rs2953441	0.83[EUR][1000 genomes]
rs4672223	0.83[EUR][1000 genomes]
rs6545663	0.83[EUR][1000 genomes]
rs6545664	0.83[EUR][1000 genomes]
rs6545665	0.83[EUR][1000 genomes]
rs6545677	0.89[CEU][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs6730037	0.82[EUR][1000 genomes]
rs6732310	0.92[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs6737913	0.81[EUR][1000 genomes]
rs6756221	0.83[EUR][1000 genomes]
rs6761347	0.83[EUR][1000 genomes]
rs7561842	0.81[EUR][1000 genomes]
rs7598169	0.83[EUR][1000 genomes]
rs908730	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs970941	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007118	chr2:57562051-58147588	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv874196	chr2:57946148-58220320	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1010981	chr2:58013389-58205699	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv874199	chr2:58031249-58161520	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv834159	chr2:58101262-58283655	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:58136400-58139400	Weak transcription	Brain Anterior Caudate	brain
2	chr2:58136600-58139800	Weak transcription	Brain Cingulate Gyrus	brain
3	chr2:58137800-58148000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr2:58138000-58140000	Weak transcription	Brain Hippocampus Middle	brain
5	chr2:58138400-58138800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:58138400-58140400	Enhancers	Brain Angular Gyrus	brain
7	chr2:58138600-58139200	Enhancers	Brain Substantia Nigra	brain

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