Variant report

Variant	rs6492616
Chromosome Location	chr13:93203349-93203350
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12874576	0.98[ASN][1000 genomes]
rs1360671	0.87[ASN][1000 genomes]
rs16947810	0.96[ASN][1000 genomes]
rs2374031	0.82[ASN][1000 genomes]
rs2780744	0.89[ASN][1000 genomes]
rs55803730	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6492610	0.82[ASN][1000 genomes]
rs6492611	0.82[ASN][1000 genomes]
rs722178	0.82[ASN][1000 genomes]
rs727986	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7490474	0.85[ASN][1000 genomes]
rs7984374	0.94[ASN][1000 genomes]
rs7984842	0.94[ASN][1000 genomes]
rs7998089	1.00[ASN][1000 genomes]
rs9561079	0.87[ASN][1000 genomes]
rs9561080	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv471168	chr13:93138577-93208593	Enhancers Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
2	nsv900904	chr13:93138577-93208593	Enhancers Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
3	nsv900905	chr13:93138577-93211339	Enhancers Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
4	nsv562728	chr13:93142706-93208593	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv456069	chr13:93161846-93204427	Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv562729	chr13:93161846-93204427	Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv818987	chr13:93201002-93208593	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93202600-93204000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr13:93203000-93203800	Weak transcription	Fetal Intestine Large	intestine

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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