Variant report

Variant	rs6930032
Chromosome Location	chr6:133015606-133015607
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs2267950	0.84[TSI][hapmap];0.80[EUR][1000 genomes]
rs2267951	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.87[TSI][hapmap];0.82[YRI][hapmap];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3798792	0.80[ASN][1000 genomes]
rs3798794	0.85[CEU][hapmap];0.82[JPT][hapmap];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3798800	0.84[TSI][hapmap];0.80[EUR][1000 genomes]
rs3798801	0.82[JPT][hapmap];0.80[EUR][1000 genomes]
rs9375912	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9389026	0.80[EUR][1000 genomes]
rs9399040	0.80[EUR][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	nsv532069	chr6:132776411-133462292	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv1015742	chr6:132933666-133285852	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6930032	SLC2A12	cis	cerebellum	SCAN

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133004800-133016400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr6:133008800-133016200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:133011800-133017200	Weak transcription	Spleen	Spleen
4	chr6:133015000-133017800	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr6:133015200-133017000	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr6:133015200-133017400	Weak transcription	Duodenum Mucosa	Duodenum
7	chr6:133015200-133019400	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr6:133015200-133019800	Weak transcription	Stomach Mucosa	stomach
9	chr6:133015400-133021200	Strong transcription	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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