Variant report

Variant	rs2835398
Chromosome Location	chr21:37968106-37968107
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 2 )

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

rs_ID	r²[population]
rs28374138	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28490337	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35210386	0.94[ASN][1000 genomes]
rs62230972	0.90[ASN][1000 genomes]
rs73206285	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9305596	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9975608	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9978893	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9981101	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9982036	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9983786	0.88[ASN][1000 genomes]
rs9983787	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9984382	1.00[CHB][hapmap];0.96[ASN][1000 genomes]
rs9984547	0.96[ASN][1000 genomes]
rs9984896	0.84[EUR][1000 genomes];0.96[ASN][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	nsv834090	chr21:37812545-38009542	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1064290	chr21:37878964-37983133	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv2762111	chr21:37967924-38023546	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2835398	BRWD1	cis	cerebellum	SCAN
rs2835398	WRB	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:37965600-37973000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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