Variant report

Variant	rs9346367
Chromosome Location	chr6:70718028-70718029
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs12110870	0.81[ASN][1000 genomes]
rs1361518	0.85[CHB][hapmap];0.80[CHD][hapmap];0.84[JPT][hapmap]
rs16868442	0.88[MEX][hapmap]
rs1934904	0.85[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2273426	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2345744	0.89[ASN][1000 genomes]
rs3793031	0.80[ASN][1000 genomes]
rs3793032	0.92[JPT][hapmap];0.80[ASN][1000 genomes]
rs3793033	0.92[JPT][hapmap];0.80[ASN][1000 genomes]
rs3793035	0.87[CHD][hapmap];0.92[JPT][hapmap];0.81[ASN][1000 genomes]
rs3793038	1.00[CEU][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3805959	0.89[CHB][hapmap];0.83[CHD][hapmap];0.84[JPT][hapmap]
rs3805963	0.90[CHB][hapmap];0.92[JPT][hapmap]
rs3805967	0.85[CHB][hapmap];0.85[CHD][hapmap];0.92[JPT][hapmap]
rs3805971	0.86[MEX][hapmap]
rs3805978	0.85[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs3805982	0.84[AMR][1000 genomes]
rs3805986	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[GIH][hapmap];0.92[LWK][hapmap];0.94[MKK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3805987	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3828766	1.00[MEX][hapmap]
rs4036075	0.85[CHB][hapmap];0.82[CHD][hapmap];0.92[JPT][hapmap]
rs56293172	0.80[ASN][1000 genomes]
rs58134065	0.81[ASN][1000 genomes]
rs59501442	0.80[ASN][1000 genomes]
rs59599861	0.80[ASN][1000 genomes]
rs6455351	0.84[CHB][hapmap];0.84[JPT][hapmap]
rs6455352	0.84[CHB][hapmap];0.92[JPT][hapmap]
rs6455353	0.89[ASN][1000 genomes]
rs6903421	0.88[CHD][hapmap];0.92[JPT][hapmap];0.80[ASN][1000 genomes]
rs6906337	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6910162	0.90[ASN][1000 genomes]
rs6912321	0.90[ASN][1000 genomes]
rs6935032	1.00[CEU][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6935585	0.85[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs6938495	0.92[JPT][hapmap]
rs73484256	0.89[ASN][1000 genomes]
rs7742627	0.84[CHD][hapmap];0.92[JPT][hapmap];0.80[ASN][1000 genomes]
rs7751448	0.85[CHB][hapmap];0.84[JPT][hapmap]
rs7756062	0.85[CHB][hapmap];0.87[CHD][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs7770758	0.99[ASN][1000 genomes]
rs7771757	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9294855	0.85[CHB][hapmap];0.84[JPT][hapmap]
rs9346368	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9351779	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs9354904	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9360410	0.85[CHB][hapmap];0.92[JPT][hapmap]
rs9364070	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9364071	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9446171	0.85[CHB][hapmap];0.80[CHD][hapmap];0.84[JPT][hapmap]
rs9446172	0.80[CHD][hapmap];0.84[JPT][hapmap]
rs9446178	0.82[AMR][1000 genomes]
rs9454912	0.90[CHB][hapmap];0.84[JPT][hapmap]
rs9454930	0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs9454932	0.90[ASN][1000 genomes]
rs9454935	0.85[CHB][hapmap];0.87[CHD][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs9454937	0.85[CHB][hapmap];0.92[JPT][hapmap];0.90[ASN][1000 genomes]
rs9454944	0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs978290	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs978291	0.81[GIH][hapmap];0.88[MEX][hapmap];0.95[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886140	chr6:70354682-70728202	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1026151	chr6:70621616-70946967	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv470832	chr6:70654657-70767756	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv603637	chr6:70658432-70740151	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv603638	chr6:70658432-70740306	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv933674	chr6:70663616-70973112	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70711800-70718600	Weak transcription	Fetal Heart	heart
2	chr6:70716200-70734000	Weak transcription	Primary B cells from cord blood	blood

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