Variant report

Variant	rs72701071
Chromosome Location	chr14:84528792-84528793
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs2787455	0.81[EUR][1000 genomes]
rs72699253	1.00[AMR][1000 genomes]
rs72699271	1.00[AMR][1000 genomes]
rs72699278	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72699280	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72699294	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72699297	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72701016	1.00[AMR][1000 genomes]
rs72701019	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72701027	1.00[AMR][1000 genomes]
rs72701031	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72701032	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72701034	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72701040	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72701043	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72701062	0.81[EUR][1000 genomes]
rs72703212	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	nsv1382	chr14:84487547-84532237	Enhancers Weak transcription Flanking Active TSS	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	chr14:84526400-84531000	Weak transcription	HUES48 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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