Variant report

Variant	rs11013910
Chromosome Location	chr10:18663370-18663371
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:10)

rs_ID	r²[population]
rs11013849	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[GIH][hapmap];0.83[TSI][hapmap];0.81[EUR][1000 genomes]
rs11013850	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[GIH][hapmap];0.81[EUR][1000 genomes]
rs12240995	0.86[CEU][hapmap];0.85[EUR][1000 genomes]
rs12780039	0.83[GIH][hapmap];1.00[MEX][hapmap];0.80[EUR][1000 genomes]
rs17610062	0.85[CEU][hapmap]
rs17610159	1.00[GIH][hapmap]
rs17683651	0.82[TSI][hapmap];0.83[EUR][1000 genomes]
rs2031571	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4748456	0.90[EUR][1000 genomes]
rs4748457	0.86[CEU][hapmap];1.00[GIH][hapmap]

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	nsv1046458	chr10:18629603-18683860	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11013910	ACBD7	cis	parietal	SCAN

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18652400-18667400	Weak transcription	Left Ventricle	heart
2	chr10:18658000-18664800	Weak transcription	Fetal Heart	heart
3	chr10:18659400-18676000	Weak transcription	Right Ventricle	heart
4	chr10:18662000-18667400	Weak transcription	Aorta	Aorta

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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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