Variant report

Variant	rs2897050
Chromosome Location	chr9:98302535-98302536
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs2405051	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28434654	0.91[EUR][1000 genomes]
rs28506778	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28508520	0.82[EUR][1000 genomes]
rs28513082	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28576382	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28637199	0.91[EUR][1000 genomes]
rs28668737	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28689133	0.91[EUR][1000 genomes]
rs28723573	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28766444	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28773488	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3847312	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3847315	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3847316	0.90[EUR][1000 genomes]
rs3858092	0.90[EUR][1000 genomes]
rs56180132	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62561361	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62561362	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531633	chr9:98078300-98431120	Flanking Active TSS Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv831658	chr9:98152971-98342178	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv430083	chr9:98204245-98445645	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv824994	chr9:98239963-98314431	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv824995	chr9:98243455-98326547	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2897050	C9orf102	cis	cerebellum	SCAN
rs2897050	OMD	cis	parietal	SCAN
rs2897050	BARX1	cis	parietal	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:98291600-98307200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:98301600-98302600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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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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