Variant report

Variant	rs9446172
Chromosome Location	chr6:70621804-70621805
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:70589300..70592044-chr6:70621641..70624143,2	K562	blood:

Extended variants
information (count: 71 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10485244	1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12110870	0.97[ASN][1000 genomes]
rs1361518	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs17766479	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1934904	0.95[CHB][hapmap];0.90[CHD][hapmap];0.84[JPT][hapmap];0.89[ASN][1000 genomes]
rs2273426	0.84[JPT][hapmap]
rs2345744	0.89[CEU][hapmap];0.89[ASN][1000 genomes]
rs3793031	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3793032	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3793033	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3793035	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.92[JPT][hapmap];0.97[ASN][1000 genomes]
rs3793036	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3805959	0.94[CHB][hapmap];0.92[CHD][hapmap];0.82[JPT][hapmap];0.97[ASN][1000 genomes]
rs3805961	0.91[CEU][hapmap];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3805962	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3805963	0.89[CHB][hapmap];0.91[JPT][hapmap];0.97[ASN][1000 genomes]
rs3805965	0.97[ASN][1000 genomes]
rs3805966	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3805967	0.95[CHB][hapmap];0.95[CHD][hapmap];0.92[JPT][hapmap];0.97[ASN][1000 genomes]
rs3805968	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3805971	0.86[MEX][hapmap];0.85[TSI][hapmap];0.95[AMR][1000 genomes]
rs3805973	0.82[CEU][hapmap];0.92[GIH][hapmap];0.87[TSI][hapmap];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3805977	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs3805978	0.91[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];0.89[ASN][1000 genomes]
rs4036075	0.95[CHB][hapmap];0.97[CHD][hapmap];0.92[JPT][hapmap];0.97[ASN][1000 genomes]
rs56293172	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56922945	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs58134065	0.97[ASN][1000 genomes]
rs59501442	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59599861	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59707679	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6455351	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6455352	0.95[CHB][hapmap];0.92[JPT][hapmap];0.97[ASN][1000 genomes]
rs6455353	0.89[ASN][1000 genomes]
rs6899719	0.92[ASN][1000 genomes]
rs6903421	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.92[JPT][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6910162	0.89[ASN][1000 genomes]
rs6912321	0.89[ASN][1000 genomes]
rs6935585	0.91[CEU][hapmap];0.95[CHB][hapmap];0.89[ASN][1000 genomes]
rs6938320	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6938495	0.84[CHB][hapmap];0.92[JPT][hapmap];0.97[ASN][1000 genomes]
rs73480070	0.97[ASN][1000 genomes]
rs73484256	0.87[ASN][1000 genomes]
rs7742627	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.92[JPT][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7751448	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7756062	0.91[CEU][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];0.89[ASN][1000 genomes]
rs7761968	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9294855	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs9346367	0.80[CHD][hapmap];0.84[JPT][hapmap]
rs9351779	0.80[JPT][hapmap]
rs9354904	0.84[JPT][hapmap]
rs9360410	0.95[CHB][hapmap];0.92[JPT][hapmap];0.97[ASN][1000 genomes]
rs9446168	0.97[ASN][1000 genomes]
rs9446169	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9446170	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9446171	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs9454908	0.97[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9454909	0.90[ASN][1000 genomes]
rs9454910	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9454912	0.89[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs9454914	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9454919	0.97[ASN][1000 genomes]
rs9454930	0.90[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];0.95[ASN][1000 genomes]
rs9454932	0.89[ASN][1000 genomes]
rs9454935	0.91[CEU][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];0.87[ASN][1000 genomes]
rs9454937	0.95[CHB][hapmap];0.88[ASN][1000 genomes]
rs9454944	0.82[CHD][hapmap];0.84[JPT][hapmap]
rs978290	0.84[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 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	nsv886141	chr6:70590638-70694162	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	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

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70605600-70627800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:70615200-70622400	Weak transcription	GM12878-XiMat	blood
3	chr6:70616400-70622400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr6:70618000-70623200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:70618000-70623400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:70618000-70624000	Weak transcription	HSMM	muscle
7	chr6:70618000-70625000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:70618200-70623600	Weak transcription	HSMMtube	muscle
9	chr6:70619600-70622400	Strong transcription	Primary B cells from cord blood	blood

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