Variant report

Variant	rs6788738
Chromosome Location	chr3:160932730-160932731
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:160926864..160930138-chr3:160930541..160935617,4	K562	blood:
2	chr3:160932675..160935542-chr3:160975472..160977359,2	K562	blood:
3	chr3:160925870..160928763-chr3:160931086..160933417,3	MCF-7	breast:
4	chr3:160932526..160936178-chr3:160936820..160939215,4	K562	blood:

Variant related genes	Relation type
ENSG00000169251	Chromatin interaction

Extended variants
information (count: 118 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs1017799	0.91[AMR][1000 genomes]
rs12489004	0.97[AMR][1000 genomes]
rs12489125	0.82[AMR][1000 genomes]
rs12490149	0.82[AMR][1000 genomes]
rs12494725	0.84[AMR][1000 genomes]
rs12496235	0.94[AMR][1000 genomes]
rs12634006	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs12634319	1.00[CEU][hapmap]
rs13315320	0.97[AMR][1000 genomes]
rs13319558	0.85[AMR][1000 genomes]
rs13319771	0.97[AMR][1000 genomes]
rs16831799	0.83[AMR][1000 genomes]
rs16831850	0.85[AMR][1000 genomes]
rs16831864	0.85[AMR][1000 genomes]
rs16831942	0.82[AMR][1000 genomes]
rs2306209	0.85[AMR][1000 genomes]
rs28451189	0.97[AMR][1000 genomes]
rs28713364	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs36015194	0.91[EUR][1000 genomes]
rs3925722	0.83[AMR][1000 genomes]
rs4296611	0.97[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs4352387	0.97[AMR][1000 genomes]
rs4468992	0.97[AMR][1000 genomes]
rs4580574	0.97[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs4635725	0.97[AMR][1000 genomes]
rs57278490	0.86[EUR][1000 genomes]
rs57496534	0.86[EUR][1000 genomes]
rs57803909	0.86[EUR][1000 genomes]
rs57903480	0.83[AMR][1000 genomes]
rs57916312	0.95[EUR][1000 genomes]
rs57974280	0.91[EUR][1000 genomes]
rs58350275	0.86[EUR][1000 genomes]
rs58562874	0.86[EUR][1000 genomes]
rs58878734	0.91[EUR][1000 genomes]
rs59371901	0.91[EUR][1000 genomes]
rs59567999	0.97[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs59593286	0.80[AMR][1000 genomes]
rs59757775	0.82[AMR][1000 genomes]
rs59761692	0.82[EUR][1000 genomes]
rs59964190	0.86[EUR][1000 genomes]
rs60612225	0.86[EUR][1000 genomes]
rs60684226	0.86[EUR][1000 genomes]
rs60866328	0.91[EUR][1000 genomes]
rs61217744	0.82[EUR][1000 genomes]
rs6441350	0.85[AMR][1000 genomes]
rs6441363	1.00[CEU][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6441365	0.97[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6441372	0.91[AMR][1000 genomes]
rs6441375	0.88[AMR][1000 genomes]
rs6762064	0.97[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6771581	0.80[AMR][1000 genomes]
rs6774919	0.97[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6775446	0.97[AMR][1000 genomes]
rs6775931	0.97[AMR][1000 genomes]
rs6778186	0.91[AMR][1000 genomes]
rs6782415	0.97[AMR][1000 genomes]
rs6782518	0.97[AMR][1000 genomes]
rs6785714	0.97[AMR][1000 genomes]
rs6787447	0.97[AMR][1000 genomes]
rs6790805	0.82[AMR][1000 genomes]
rs6796168	0.83[AMR][1000 genomes]
rs6798468	0.91[EUR][1000 genomes]
rs6801664	0.97[AMR][1000 genomes]
rs6805976	0.97[AMR][1000 genomes]
rs73017340	0.91[AMR][1000 genomes]
rs73023224	0.91[EUR][1000 genomes]
rs73026933	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs73026967	0.97[AMR][1000 genomes]
rs73026968	0.97[AMR][1000 genomes]
rs73026983	0.97[AMR][1000 genomes]
rs73026987	0.97[AMR][1000 genomes]
rs73026989	0.97[AMR][1000 genomes]
rs73878307	0.82[EUR][1000 genomes]
rs73878308	0.82[EUR][1000 genomes]
rs73878309	0.85[AMR][1000 genomes]
rs73878311	0.82[EUR][1000 genomes]
rs7615833	0.97[AMR][1000 genomes]
rs7615868	0.94[AMR][1000 genomes]
rs7624791	0.91[AMR][1000 genomes]
rs7625217	0.86[EUR][1000 genomes]
rs7626773	0.91[AMR][1000 genomes]
rs7634299	0.97[AMR][1000 genomes]
rs7651924	0.88[AMR][1000 genomes]
rs7652624	0.91[AMR][1000 genomes]
rs873183	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs896080	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs9290070	0.97[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs9290071	0.97[AMR][1000 genomes]
rs9682249	0.83[AMR][1000 genomes]
rs9812574	0.91[AMR][1000 genomes]
rs9818470	0.91[AMR][1000 genomes]
rs9819793	0.97[AMR][1000 genomes]
rs9822705	0.85[AMR][1000 genomes]
rs9822916	0.97[AMR][1000 genomes]
rs9824805	0.97[AMR][1000 genomes]
rs9830183	0.94[AMR][1000 genomes]
rs9833270	0.88[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs9834806	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9835530	0.85[AMR][1000 genomes]
rs9838945	0.91[AMR][1000 genomes]
rs9841871	0.97[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs9842290	0.91[AMR][1000 genomes]
rs9847842	0.97[AMR][1000 genomes]
rs9851699	0.82[AMR][1000 genomes]
rs9855112	0.94[AMR][1000 genomes]
rs9855572	0.88[AMR][1000 genomes]
rs9856742	0.97[AMR][1000 genomes]
rs9859641	0.97[AMR][1000 genomes]
rs9860980	0.85[AMR][1000 genomes]
rs9862867	0.91[AMR][1000 genomes]
rs9871753	0.97[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs9876077	0.91[AMR][1000 genomes]
rs9877309	0.97[AMR][1000 genomes]
rs9880536	0.91[AMR][1000 genomes]
rs9884100	0.97[AMR][1000 genomes]
rs9985364	0.97[AMR][1000 genomes];0.80[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	nsv931072	chr3:160669567-161159779	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv1015063	chr3:160918307-161024070	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160926000-160938400	Weak transcription	Brain Substantia Nigra	brain
2	chr3:160931000-160938600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr3:160931400-160935200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr3:160931800-160937200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr3:160931800-160938400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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