Variant report

Variant	rs2907393
Chromosome Location	chr17:66604445-66604446
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 4 )

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

rs_ID	r²[population]
rs12150134	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2159332	0.82[EUR][1000 genomes]
rs2907392	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2952303	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2952304	0.81[ASN][1000 genomes]
rs2952310	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4968905	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4968906	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58171668	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs67000278	0.83[ASN][1000 genomes]
rs7219279	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9915019	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833524	chr17:66524030-66705194	Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs2907393	ARSG	cis	cerebellum	SCAN
rs2907393	CYB561	cis	parietal	SCAN
rs2907393	SNORA38B	cis	parietal	SCAN
rs2907393	SMARCD2	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66602200-66605800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
2	chr17:66603200-66604600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
3	chr17:66604000-66606800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
4	chr17:66604000-66607200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr17:66604200-66607000	ZNF genes & repeats	Liver	Liver

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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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