Variant report

Variant	rs2699759
Chromosome Location	chr7:118502973-118502974
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1357576	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1916717	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1919915	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1919919	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2204779	1.00[EUR][1000 genomes]
rs2222496	1.00[EUR][1000 genomes]
rs2246466	1.00[EUR][1000 genomes]
rs2256842	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2263400	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2440896	1.00[EUR][1000 genomes]
rs2590593	1.00[EUR][1000 genomes]
rs2590602	1.00[EUR][1000 genomes]
rs2590645	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2590650	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2689718	1.00[EUR][1000 genomes]
rs2699700	1.00[EUR][1000 genomes]
rs2699701	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2699705	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2699706	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2699707	1.00[EUR][1000 genomes]
rs2699749	0.90[AMR][1000 genomes]
rs2699755	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2699756	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2699757	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2699766	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs2699767	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs2699768	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2699769	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2699770	1.00[EUR][1000 genomes]
rs6974190	0.81[AMR][1000 genomes];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	nsv889093	chr7:117977091-118709754	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv889096	chr7:118438184-118709754	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1021902	chr7:118452600-118719244	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv889097	chr7:118458421-118634585	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr7:118501600-118504400	Enhancers	Fetal Stomach	stomach

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