Variant report

Variant	rs61902021
Chromosome Location	chr11:56210194-56210195
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs12272629	0.83[EUR][1000 genomes]
rs17541821	0.89[EUR][1000 genomes]
rs17541876	0.89[EUR][1000 genomes]
rs17546536	0.98[EUR][1000 genomes]
rs17613345	0.83[EUR][1000 genomes]
rs17627302	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17628586	1.00[EUR][1000 genomes]
rs17628691	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17629033	0.98[EUR][1000 genomes]
rs17629218	0.98[EUR][1000 genomes]
rs1807254	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55706115	0.89[EUR][1000 genomes]
rs55771448	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56077409	0.89[EUR][1000 genomes]
rs56078926	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs56163075	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56394926	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61888282	0.83[EUR][1000 genomes]
rs61888286	0.83[EUR][1000 genomes]
rs61888289	0.83[EUR][1000 genomes]
rs61888309	0.83[EUR][1000 genomes]
rs61888312	0.83[EUR][1000 genomes]
rs61888313	0.83[EUR][1000 genomes]
rs61901983	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61902022	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61902171	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs61902203	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs61902209	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs61902863	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61902883	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61902885	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61902915	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61902916	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61902921	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61903268	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs61903273	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs61903478	0.85[EUR][1000 genomes]
rs61903482	0.86[EUR][1000 genomes]
rs61903483	0.86[EUR][1000 genomes]
rs61903484	0.89[EUR][1000 genomes]
rs61903485	0.89[EUR][1000 genomes]
rs61903486	0.89[EUR][1000 genomes]
rs61903487	0.89[EUR][1000 genomes]
rs61903530	0.88[EUR][1000 genomes]
rs61903531	0.88[EUR][1000 genomes]
rs61903536	0.88[EUR][1000 genomes]
rs61903537	0.88[EUR][1000 genomes]
rs61903541	0.88[EUR][1000 genomes]
rs61904062	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs61904063	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs61904064	0.98[EUR][1000 genomes]
rs6591380	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs7103598	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7106248	0.89[EUR][1000 genomes]
rs7114870	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs7121384	0.89[EUR][1000 genomes]
rs7121385	0.89[EUR][1000 genomes]
rs7121991	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7124023	0.89[EUR][1000 genomes]
rs7125690	0.80[EUR][1000 genomes]
rs7126549	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7130906	0.98[EUR][1000 genomes]
rs716103	0.83[EUR][1000 genomes]
rs716104	0.83[EUR][1000 genomes]
rs7932621	0.83[EUR][1000 genomes]
rs7951134	0.83[EUR][1000 genomes]
rs7951506	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050024	chr11:55900482-56518943	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	52 gene(s)	inside rSNPs	diseases
2	nsv497854	chr11:55917298-56537994	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
3	nsv555096	chr11:56084444-56235061	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
4	nsv555097	chr11:56084611-56235061	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
5	nsv971949	chr11:56126625-56344170	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56210000-56210800	Enhancers	Fetal Intestine Large	intestine

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