Variant report

Variant	rs2865775
Chromosome Location	chr4:97963926-97963927
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11936118	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13116809	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13121156	0.81[ASN][1000 genomes]
rs17247656	0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs17247873	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35203848	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4141304	0.95[ASN][1000 genomes]
rs56120140	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61051836	0.83[ASN][1000 genomes]
rs6840021	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs6840385	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7673377	0.81[ASN][1000 genomes]
rs981544	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879640	chr4:97711707-98697586	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1005103	chr4:97914293-98011695	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2865775	EMCN	cis	cerebellum	SCAN
rs2865775	ADH1A	cis	cerebellum	SCAN

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:97959400-97965600	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr4:97959800-97964000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr4:97960000-97966000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr4:97963800-97964200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr4:97963800-97964400	Enhancers	Dnd41	blood

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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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