Variant report

Variant	rs1924084
Chromosome Location	chr9:10325732-10325733
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10118721	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs10123173	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10756025	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10756026	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10756028	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10809070	0.83[AMR][1000 genomes]
rs10959043	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10959045	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10959048	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs10959049	0.81[AMR][1000 genomes]
rs10959050	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs12000957	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12000959	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7849722	0.80[AMR][1000 genomes]
rs7851619	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7854874	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9657580	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9987444	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9987798	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9987808	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9987891	0.93[EUR][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	nsv1034731	chr9:9776126-10481262	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv892295	chr9:9832245-10380406	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1030657	chr9:10002355-10481262	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1033178	chr9:10169848-10428731	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2758179	chr9:10188450-10370398	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2759666	chr9:10188450-10370398	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1033020	chr9:10314941-10330352	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv2764134	chr9:10314941-10330364	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv516073	chr9:10314941-10333382	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:10323600-10330200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr9:10324400-10326000	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr9:10325000-10325800	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr9:10325000-10325800	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr9:10325200-10325800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr9:10325400-10330800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr9:10325400-10331200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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