Variant report

Variant	rs35222380
Chromosome Location	chr9:78879550-78879551
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs34308090	1.00[AMR][1000 genomes]
rs34676706	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34700268	1.00[AFR][1000 genomes]
rs34750481	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34954896	0.85[AFR][1000 genomes]
rs34968508	0.85[AFR][1000 genomes]
rs35047237	1.00[AMR][1000 genomes]
rs35124462	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35154668	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35570750	1.00[AMR][1000 genomes]
rs35948094	1.00[AMR][1000 genomes]
rs7811545	1.00[AFR][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	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	nsv893476	chr9:78768830-78887992	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
3	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
4	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	chr9:78855800-78881800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr9:78872800-78881600	Weak transcription	Ovary	ovary
3	chr9:78875600-78881600	Weak transcription	Fetal Intestine Small	intestine
4	chr9:78876200-78891400	Weak transcription	Duodenum Mucosa	Duodenum

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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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