Variant report

Variant	rs13439871
Chromosome Location	chr8:91444580-91444581
allele	A/T
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]
rs10086788	0.86[EUR][1000 genomes]
rs10087100	0.93[EUR][1000 genomes]
rs10099647	0.86[EUR][1000 genomes]
rs10100923	0.89[EUR][1000 genomes]
rs10103125	0.86[EUR][1000 genomes]
rs10103138	0.96[EUR][1000 genomes]
rs10104445	0.93[EUR][1000 genomes]
rs10104451	0.86[EUR][1000 genomes]
rs10106274	0.93[EUR][1000 genomes]
rs10111531	0.86[EUR][1000 genomes]
rs10112375	0.93[EUR][1000 genomes]
rs10112676	0.86[EUR][1000 genomes]
rs10156381	0.83[EUR][1000 genomes]
rs1015844	0.93[EUR][1000 genomes]
rs10216873	0.93[EUR][1000 genomes]
rs16904545	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs28385552	0.89[EUR][1000 genomes]
rs28550265	0.93[EUR][1000 genomes]
rs28610968	0.83[EUR][1000 genomes]
rs28684622	0.93[EUR][1000 genomes]
rs28882092	0.93[EUR][1000 genomes]
rs58836045	0.86[EUR][1000 genomes]
rs9297838	0.93[EUR][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	esv3413614	chr8:91444326-91448524	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91441000-91445800	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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