Variant report

Variant	rs9869649
Chromosome Location	chr3:155854433-155854434
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:155853531..155854523-chr3:156102494..156103055,2	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10936024	1.00[CHB][hapmap];0.84[JPT][hapmap];0.97[ASN][1000 genomes]
rs11709514	1.00[CHB][hapmap];0.84[JPT][hapmap];0.92[ASN][1000 genomes]
rs11716256	0.92[ASN][1000 genomes]
rs11718399	1.00[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs12493813	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13073556	1.00[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs13093154	0.94[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs1488425	1.00[CHB][hapmap];0.82[JPT][hapmap];0.92[ASN][1000 genomes]
rs1488426	0.85[ASN][1000 genomes]
rs4234308	0.81[CEU][hapmap];0.87[CHB][hapmap];0.83[JPT][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4261831	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs4359773	0.91[ASN][1000 genomes]
rs4359774	0.88[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs4605502	0.94[CHB][hapmap];0.91[ASN][1000 genomes]
rs4679760	0.91[ASN][1000 genomes]
rs4679761	0.94[CHB][hapmap];0.84[JPT][hapmap];0.88[ASN][1000 genomes]
rs4680231	0.80[EUR][1000 genomes]
rs4680232	1.00[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs4680233	1.00[CHB][hapmap];0.83[JPT][hapmap];0.96[ASN][1000 genomes]
rs4680234	0.93[ASN][1000 genomes]
rs4680235	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4680237	0.94[CHB][hapmap];0.84[JPT][hapmap];0.91[ASN][1000 genomes]
rs56231269	0.97[ASN][1000 genomes]
rs62284939	0.97[ASN][1000 genomes]
rs6441034	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6441035	0.94[CHB][hapmap];0.91[ASN][1000 genomes]
rs6441036	0.84[CEU][hapmap];0.94[CHB][hapmap];0.85[JPT][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6761966	0.83[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6778035	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6778199	0.81[EUR][1000 genomes]
rs6780500	0.99[ASN][1000 genomes]
rs6788449	1.00[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs6793964	1.00[CHB][hapmap];0.84[JPT][hapmap];0.97[ASN][1000 genomes]
rs7617796	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7618820	0.88[CHB][hapmap];0.91[ASN][1000 genomes]
rs7629439	0.83[CEU][hapmap];0.94[CHB][hapmap];0.91[JPT][hapmap];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7633081	0.97[ASN][1000 genomes]
rs9289961	1.00[CHB][hapmap];0.92[ASN][1000 genomes]
rs9683366	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9814661	0.94[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs9816126	0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9838322	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9842620	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs9856468	0.94[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs9861320	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs9862153	1.00[CHB][hapmap];0.84[JPT][hapmap];0.97[ASN][1000 genomes]
rs9862554	0.80[CEU][hapmap]
rs9870793	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9882088	0.94[CHB][hapmap];0.88[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv592085	chr3:155827634-156012679	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155850400-155857200	Weak transcription	Ovary	ovary
2	chr3:155850400-155861800	Weak transcription	Right Atrium	heart
3	chr3:155851600-155856600	Weak transcription	Fetal Muscle Leg	muscle
4	chr3:155852800-155856800	Enhancers	Aorta	Aorta

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