Variant report

Variant	rs1332291
Chromosome Location	chr9:6124101-6124102
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10739084	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1332292	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1537285	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1556470	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1591044	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs168168	0.90[EUR][1000 genomes]
rs1755531	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs189348	0.81[EUR][1000 genomes]
rs1970089	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2150969	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs340887	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs340893	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs340894	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs340896	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs340901	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs340902	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs340903	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs340904	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs340905	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs340906	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs340918	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs340919	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs340921	0.88[EUR][1000 genomes]
rs340922	0.88[EUR][1000 genomes]
rs340923	0.90[EUR][1000 genomes]
rs340924	0.90[EUR][1000 genomes]
rs340925	0.88[EUR][1000 genomes]
rs340926	0.89[EUR][1000 genomes]
rs340933	0.90[EUR][1000 genomes]
rs340934	0.81[EUR][1000 genomes]
rs340935	0.81[EUR][1000 genomes]
rs343475	0.81[EUR][1000 genomes]
rs343476	0.81[EUR][1000 genomes]
rs343496	0.81[EUR][1000 genomes]
rs369996	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs371165	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs371454	0.84[EUR][1000 genomes]
rs372560	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs374672	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs375560	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs376690	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs378952	0.82[EUR][1000 genomes]
rs380888	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs390158	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs394879	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs397916	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs398561	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs399834	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs401731	0.84[EUR][1000 genomes]
rs401834	0.84[EUR][1000 genomes]
rs413382	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs420445	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs425489	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs437389	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs441616	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs442851	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs443175	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs503384	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs503507	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs531759	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62558390	0.81[EUR][1000 genomes]
rs639247	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs694796	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs695013	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7850455	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs821164	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9407312	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9407324	0.86[AMR][1000 genomes]
rs9408638	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs974936	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948847	chr9:5712626-6417677	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv1031086	chr9:5806949-6630686	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv539967	chr9:5806949-6630686	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv613205	chr9:6032924-6332901	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv916394	chr9:6055497-6322471	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv2761482	chr9:6084602-6134787	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv892157	chr9:6093790-6322415	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv933124	chr9:6099101-6644738	Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
9	nsv831496	chr9:6101763-6285088	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr9:6123400-6124400	Enhancers	Psoas Muscle	Psoas
2	chr9:6123600-6124400	Weak transcription	Spleen	Spleen
3	chr9:6123800-6124200	Enhancers	Fetal Muscle Leg	muscle
4	chr9:6123800-6124200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
5	chr9:6124000-6124400	Enhancers	Skeletal Muscle Male	skeletal muscle

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