Variant report

Variant	rs9485584
Chromosome Location	chr6:102464109-102464110
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs73763641	0.95[AFR][1000 genomes]
rs9322622	1.00[YRI][hapmap]
rs9485566	1.00[YRI][hapmap]
rs9485578	1.00[YRI][hapmap]
rs9485580	1.00[YRI][hapmap]
rs9485590	1.00[YRI][hapmap]
rs9498759	1.00[YRI][hapmap]
rs9498779	1.00[YRI][hapmap]
rs9498790	1.00[YRI][hapmap]
rs9498791	1.00[YRI][hapmap]
rs9498793	1.00[YRI][hapmap]
rs9498795	0.83[AFR][1000 genomes]
rs9498802	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9498803	1.00[YRI][hapmap]
rs9498804	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9498813	1.00[YRI][hapmap]
rs9498815	1.00[YRI][hapmap]
rs9498816	1.00[YRI][hapmap]
rs9498822	1.00[YRI][hapmap]
rs9498823	1.00[YRI][hapmap]
rs9986426	1.00[YRI][hapmap];1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032499	chr6:102069885-102720998	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv886465	chr6:102318339-102466397	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv470850	chr6:102343078-102595587	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv830744	chr6:102369761-102566737	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1033919	chr6:102417713-102474539	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2756012	chr6:102428797-102489159	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:102463000-102471400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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