Variant report

Variant	rs7119614
Chromosome Location	chr11:56102827-56102828
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs17541821	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs17541876	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs17613345	1.00[AFR][1000 genomes]
rs17614327	0.81[CEU][hapmap]
rs1945237	0.81[CEU][hapmap]
rs1947923	0.81[CEU][hapmap]
rs55706115	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs55892403	1.00[AFR][1000 genomes]
rs56077409	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs56149224	1.00[AFR][1000 genomes]
rs61887243	1.00[AFR][1000 genomes]
rs61888289	1.00[AFR][1000 genomes]
rs61888312	1.00[AFR][1000 genomes]
rs61888313	1.00[AFR][1000 genomes]
rs61903478	1.00[AFR][1000 genomes]
rs61903482	1.00[AFR][1000 genomes]
rs61903484	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs61903485	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs61903486	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs61903487	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs61903530	0.81[EUR][1000 genomes]
rs61903531	0.81[EUR][1000 genomes]
rs61903536	0.81[EUR][1000 genomes]
rs61903537	0.81[EUR][1000 genomes]
rs61903541	0.81[EUR][1000 genomes]
rs7106248	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs7111634	0.81[CEU][hapmap]
rs7114870	0.81[CEU][hapmap]
rs7119253	0.81[CEU][hapmap]
rs7121384	0.83[EUR][1000 genomes]
rs7121385	0.83[EUR][1000 genomes]
rs7123108	0.81[CEU][hapmap]
rs7124023	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs7125690	0.81[CEU][hapmap]

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	nsv975114	chr11:55751535-56124251	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
2	nsv1044859	chr11:55900482-56121727	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	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
4	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
5	nsv832161	chr11:56046173-56166964	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
6	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
7	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56097200-56104800	Weak transcription	H1 Cell Line	embryonic stem cell

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