Variant report

Variant	rs6959913
Chromosome Location	chr7:49933913-49933914
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10237792	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10249896	1.00[AMR][1000 genomes]
rs1483075	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1532990	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2128940	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs503212	0.83[AFR][1000 genomes]
rs523562	0.83[AFR][1000 genomes]
rs55803220	1.00[AMR][1000 genomes]
rs581181	0.83[AFR][1000 genomes]
rs624007	0.83[AFR][1000 genomes]
rs655184	0.84[AFR][1000 genomes]
rs73336269	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73347089	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73349124	1.00[AMR][1000 genomes]
rs9886120	0.98[AFR][1000 genomes];1.00[AMR][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	nsv464444	chr7:49671882-50454736	Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv606897	chr7:49671883-50454736	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv498090	chr7:49708644-50427714	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1020869	chr7:49712860-50457544	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 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	chr7:49933600-49934600	Enhancers	Ovary	ovary
2	chr7:49933800-49934800	Enhancers	Left Ventricle	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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