Variant report

Variant	rs35472604
Chromosome Location	chr9:3618802-3618803
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:72)

rs_ID	r²[population]
rs10512866	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11951477	0.87[EUR][1000 genomes]
rs11957933	0.87[EUR][1000 genomes]
rs13153376	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13153426	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13162944	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13163070	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13165641	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13165992	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13166622	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13167135	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13167593	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13172191	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13173899	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13180428	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13183825	0.87[EUR][1000 genomes]
rs13184849	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13185697	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13187122	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13187187	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13188873	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13188895	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16901939	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16901954	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16901958	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16901986	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16901987	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2330571	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34094652	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34098474	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34133773	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34172556	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34216230	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34282174	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34544432	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34918593	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34942360	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35241613	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35278372	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35534193	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35564441	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35842403	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35850760	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35868527	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36163058	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4398644	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57288883	0.87[EUR][1000 genomes]
rs58871041	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59337658	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60303396	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60772043	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61695869	1.00[ASN][1000 genomes]
rs6451785	0.87[EUR][1000 genomes]
rs6860030	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6869608	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6870104	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6870510	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6876888	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6877331	0.87[EUR][1000 genomes]
rs6877454	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6881573	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6882983	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6891637	0.87[EUR][1000 genomes]
rs6893211	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71590654	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73752417	1.00[ASN][1000 genomes]
rs73752418	1.00[ASN][1000 genomes]
rs7704815	0.87[EUR][1000 genomes]
rs7710153	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7726555	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7735466	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7736197	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916259	chr9:3308176-4296711	Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
2	nsv1022795	chr9:3436845-3744623	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
3	nsv892092	chr9:3565211-3687942	Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1033417	chr9:3594189-3732530	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1021394	chr9:3594389-3728995	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1032487	chr9:3601907-3661151	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv892093	chr9:3613712-3696874	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:3600800-3620400	Weak transcription	Ovary	ovary
2	chr9:3606400-3640400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr9:3611600-3628000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr9:3613600-3619600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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