Variant report

Variant	rs10133673
Chromosome Location	chr14:37537352-37537353
allele	C/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:70)

rs_ID	r²[population]
rs1012199	0.93[CHB][hapmap];0.92[JPT][hapmap]
rs10132328	0.91[ASN][1000 genomes]
rs10136238	1.00[ASN][1000 genomes]
rs10141752	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10142021	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10151092	0.93[CHB][hapmap];0.85[JPT][hapmap]
rs10220281	0.89[ASN][1000 genomes]
rs10220604	0.93[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10459480	0.93[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];1.00[TSI][hapmap]
rs10483482	1.00[TSI][hapmap]
rs10483485	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11156929	1.00[TSI][hapmap]
rs12050169	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12050463	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12232098	1.00[TSI][hapmap]
rs12590281	1.00[TSI][hapmap]
rs12889634	0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs17091939	0.85[CHB][hapmap];1.00[TSI][hapmap]
rs17105957	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17106031	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs17106189	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17106209	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17106216	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17106275	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17106290	0.93[CHB][hapmap];0.97[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.91[ASN][1000 genomes]
rs17106291	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17106309	0.90[CHB][hapmap];0.92[JPT][hapmap]
rs17106333	0.85[CHB][hapmap];0.92[JPT][hapmap];1.00[EUR][1000 genomes]
rs17106347	0.82[CHD][hapmap];0.83[GIH][hapmap]
rs17106393	0.93[CHB][hapmap];0.92[JPT][hapmap]
rs17106396	0.93[CHB][hapmap];0.92[JPT][hapmap]
rs17106404	0.93[CHB][hapmap];0.92[JPT][hapmap]
rs17106433	0.93[CHB][hapmap];0.92[JPT][hapmap]
rs17106509	0.85[CHB][hapmap];1.00[TSI][hapmap]
rs17106512	0.91[CHB][hapmap]
rs17841015	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17841017	1.00[EUR][1000 genomes]
rs1884220	0.91[ASN][1000 genomes]
rs1884221	0.93[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1884775	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1884777	0.93[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1950376	0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1950814	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1955760	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1955761	0.93[CHB][hapmap];0.92[JPT][hapmap]
rs1955763	0.93[CHB][hapmap];0.83[JPT][hapmap]
rs1956423	0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1956424	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1998121	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2057171	0.91[ASN][1000 genomes]
rs2078246	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];0.85[JPT][hapmap];1.00[TSI][hapmap]
rs2415379	0.93[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2415380	0.92[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2415385	0.82[CHD][hapmap]
rs2415388	0.92[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap]
rs28517624	1.00[ASN][1000 genomes]
rs28593311	1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4356385	0.95[ASN][1000 genomes]
rs4900678	0.82[CHD][hapmap]
rs7140991	0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7151524	0.93[CHB][hapmap];0.92[JPT][hapmap]
rs7153409	0.82[CHD][hapmap]
rs7160129	0.93[CHB][hapmap];0.85[JPT][hapmap]
rs74045463	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs74045478	0.91[ASN][1000 genomes]
rs8008478	0.93[CHB][hapmap];0.97[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.91[ASN][1000 genomes]
rs8014186	0.93[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs8019489	0.93[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs8020153	0.91[ASN][1000 genomes]
rs9888585	1.00[GIH][hapmap]

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	nsv534288	chr14:37254539-37697745	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1036201	chr14:37498841-37542041	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1037719	chr14:37498841-37546359	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv526786	chr14:37499904-37537352	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1048854	chr14:37505438-37546359	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37527200-37539800	Weak transcription	Muscle Satellite Cultured Cells	--

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