Variant report

Variant	rs9322088
Chromosome Location	chr6:147393466-147393467
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:147391002..147395270-chr6:147401582..147403609,4	K562	blood:
2	chr6:147392966..147394891-chr6:147523665..147525984,2	K562	blood:
3	chr6:147391588..147394483-chr6:147471638..147473937,2	K562	blood:

Variant related genes	Relation type
ENSG00000164506	Chromatin interaction
ENSG00000233452	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1105441	0.81[AMR][1000 genomes]
rs12209736	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1529016	0.86[CHB][hapmap]
rs1881660	0.88[CEU][hapmap];0.91[MEX][hapmap];0.89[TSI][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2256216	0.83[MEX][hapmap]
rs2328803	0.80[AMR][1000 genomes]
rs3734477	0.89[CEU][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4896903	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6570788	0.81[AMR][1000 genomes]
rs6570789	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6901138	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6910250	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6920096	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6920901	0.87[MEX][hapmap];0.82[TSI][hapmap]
rs6924131	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6930740	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7749744	0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];0.91[TSI][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7755338	0.89[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7767185	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7772651	0.86[CHB][hapmap]
rs9322089	0.92[CEU][hapmap];0.88[CHD][hapmap];0.91[GIH][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9377043	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9377044	0.81[AMR][1000 genomes]
rs9377045	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9386178	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9403845	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9485141	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9497685	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9497690	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]

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	nsv1019245	chr6:147350834-147609776	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv538467	chr6:147350834-147609776	Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv886751	chr6:147354092-147490398	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147387000-147396600	Weak transcription	Brain Anterior Caudate	brain
2	chr6:147391200-147398400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr6:147392600-147393600	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr6:147392600-147393800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr6:147393000-147395000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:147393400-147400600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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