Variant report

Variant	rs17628691
Chromosome Location	chr11:56253820-56253821
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 95 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10501355	0.84[EUR][1000 genomes]
rs17541821	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs17541876	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs17542961	1.00[CEU][hapmap]
rs17546536	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17547207	1.00[CEU][hapmap]
rs17547284	1.00[CEU][hapmap]
rs17547542	1.00[CEU][hapmap]
rs17547806	1.00[CEU][hapmap]
rs17548679	0.92[EUR][1000 genomes]
rs17548700	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17548819	1.00[CEU][hapmap]
rs17613345	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs17614327	1.00[CEU][hapmap]
rs17627302	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17628586	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17629033	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17629218	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17629804	1.00[CEU][hapmap]
rs17629861	1.00[CEU][hapmap]
rs17630028	1.00[CEU][hapmap]
rs17630040	0.91[CEU][hapmap]
rs1807254	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1876924	1.00[CEU][hapmap]
rs1945237	1.00[CEU][hapmap]
rs1945262	1.00[CEU][hapmap]
rs55706115	0.89[EUR][1000 genomes]
rs55771448	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55874240	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56077409	0.89[EUR][1000 genomes]
rs56078926	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56163075	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56394926	1.00[AMR][1000 genomes];0.94[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	0.98[EUR][1000 genomes]
rs61902021	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61902022	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61902171	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61902203	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61902209	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61902863	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61902883	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61902885	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61902915	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61902916	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61902921	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61903268	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61903273	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61903306	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61903313	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61903315	0.84[EUR][1000 genomes]
rs61903316	0.82[EUR][1000 genomes]
rs61903320	0.84[EUR][1000 genomes]
rs61903321	0.84[EUR][1000 genomes]
rs61903347	0.81[AMR][1000 genomes];0.84[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	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61904063	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61904064	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6591380	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7103598	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7106248	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs7111634	1.00[CEU][hapmap]
rs7114870	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7121384	0.89[EUR][1000 genomes]
rs7121385	0.89[EUR][1000 genomes]
rs7121991	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7123108	1.00[CEU][hapmap]
rs7124023	0.89[EUR][1000 genomes]
rs7126549	1.00[EUR][1000 genomes]
rs7130906	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7925450	1.00[CEU][hapmap]
rs7927015	0.91[CEU][hapmap]
rs7935533	1.00[CEU][hapmap]
rs7939771	0.84[EUR][1000 genomes]
rs7942730	1.00[CEU][hapmap]
rs7951506	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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	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
4	nsv1046487	chr11:56228761-56310644	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56253200-56256200	Enhancers	Fetal Intestine Small	intestine
2	chr11:56253600-56256400	Enhancers	Fetal Intestine Large	intestine

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