Variant report

Variant	rs6964017
Chromosome Location	chr7:127104822-127104823
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10246965	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10252007	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10260068	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10279972	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10487478	1.00[AMR][1000 genomes]
rs11563297	1.00[AMR][1000 genomes]
rs11563458	1.00[AMR][1000 genomes]
rs11563461	1.00[AMR][1000 genomes]
rs11563469	1.00[AMR][1000 genomes]
rs11563471	1.00[AMR][1000 genomes]
rs1419417	1.00[AMR][1000 genomes]
rs1557641	1.00[AMR][1000 genomes]
rs17150923	0.90[AFR][1000 genomes]
rs17864971	1.00[AMR][1000 genomes]
rs17865209	1.00[AMR][1000 genomes]
rs17865399	1.00[AMR][1000 genomes]
rs17865903	1.00[AMR][1000 genomes]
rs17865905	1.00[AMR][1000 genomes]
rs17866001	1.00[AMR][1000 genomes]
rs17866216	1.00[AMR][1000 genomes]
rs17866217	1.00[AMR][1000 genomes]
rs17870051	1.00[AMR][1000 genomes]
rs2040501	1.00[AMR][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	esv1820283	chr7:127101187-127110765	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127097400-127116000	Weak transcription	Pancreas	Pancrea

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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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