Variant report

Variant	rs735859
Chromosome Location	chr6:164392968-164392969
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	chr6:164386071..164388210-chr6:164391246..164393203,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10428875	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10484512	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10484513	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10484514	0.90[EUR][1000 genomes]
rs10484515	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10945938	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10945939	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10945940	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10945941	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10945942	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10945944	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10945945	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12189842	0.82[ASN][1000 genomes]
rs12209088	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12209089	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13193552	0.89[EUR][1000 genomes]
rs1545107	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34021940	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34091550	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34413611	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34561573	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34727935	0.90[EUR][1000 genomes]
rs34994154	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35668088	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4304140	0.88[EUR][1000 genomes]
rs4709799	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4709800	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4709802	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4709803	0.82[AMR][1000 genomes]
rs551475	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62435513	0.90[EUR][1000 genomes]
rs62435541	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6455930	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6455931	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs735858	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7754718	0.85[ASN][1000 genomes]
rs9356176	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9364711	0.86[EUR][1000 genomes]
rs942009	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][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	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1026707	chr6:164188210-164749206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv538527	chr6:164188210-164749206	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv830858	chr6:164296054-164455743	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv5582	chr6:164390353-164405727	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164380000-164393600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:164380800-164393000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:164387000-164393000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:164387400-164393200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr6:164389200-164404600	Weak transcription	Fetal Heart	heart
6	chr6:164392200-164393200	Enhancers	Placenta	Placenta
7	chr6:164392400-164393000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:164392800-164393600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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