Variant report

Variant	rs1971243
Chromosome Location	chr14:84617069-84617070
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11627572	0.83[ASN][1000 genomes]
rs11628862	1.00[AFR][1000 genomes]
rs12895378	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1381621	0.81[EUR][1000 genomes]
rs1564058	0.82[EUR][1000 genomes]
rs17624404	0.88[ASN][1000 genomes]
rs17697962	1.00[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4904160	0.82[EUR][1000 genomes]
rs4904161	0.81[EUR][1000 genomes]
rs67901677	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72703208	1.00[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs72703211	0.88[ASN][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	nsv565376	chr14:84612088-84644822	Enhancers Weak transcription	TF binding region lncRNA	3 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	chr14:84615800-84618600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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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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