Variant report

Variant	rs10279752
Chromosome Location	chr7:102906637-102906638
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10046531	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10234196	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10235693	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10241815	1.00[AMR][1000 genomes]
rs10243055	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10245037	1.00[AMR][1000 genomes]
rs10246237	1.00[AMR][1000 genomes]
rs10252006	1.00[AMR][1000 genomes]
rs10255884	1.00[AMR][1000 genomes]
rs10258184	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10259126	1.00[AMR][1000 genomes]
rs10271644	1.00[AMR][1000 genomes]
rs10273102	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10279918	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10441305	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2079253	0.90[AFR][1000 genomes]
rs28399298	1.00[AMR][1000 genomes]
rs28452903	1.00[AMR][1000 genomes]
rs28482805	1.00[AMR][1000 genomes]
rs28605237	1.00[AMR][1000 genomes]
rs28894762	1.00[AMR][1000 genomes]
rs4480048	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4612274	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56703102	1.00[AMR][1000 genomes]
rs58192762	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6944594	1.00[AMR][1000 genomes]
rs6951111	1.00[AMR][1000 genomes]
rs6953456	1.00[AMR][1000 genomes]
rs7794374	0.90[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	nsv868996	chr7:102332827-102991361	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv831084	chr7:102778908-102964970	Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	esv1794417	chr7:102814101-102928545	Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv981567	chr7:102850992-102924834	Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr7:102906200-102907000	Enhancers	K562	blood
2	chr7:102906600-102907600	Enhancers	Fetal Heart	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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