Variant report

Variant	rs7037592
Chromosome Location	chr9:78889852-78889853
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:16)

rs_ID	r²[population]
rs10122766	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12335946	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12345311	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12345402	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12345405	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17062309	0.94[AFR][1000 genomes]
rs17062312	0.94[AFR][1000 genomes]
rs17062335	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28725352	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57722010	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7041259	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7041527	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73652909	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73652910	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73652911	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73652912	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869152	chr9:78742197-79583399	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv931033	chr9:78850330-79366454	Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv508552	chr9:78864913-78956326	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:78876200-78891400	Weak transcription	Duodenum Mucosa	Duodenum
2	chr9:78883000-78917200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr9:78889600-78893200	Strong transcription	Fetal Intestine Small	intestine
4	chr9:78889800-78893400	Strong transcription	Fetal Intestine Large	intestine

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Input of quick search could be:

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

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