Variant report

Variant	rs72703212
Chromosome Location	chr14:84596994-84596995
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs72699253	1.00[AMR][1000 genomes]
rs72699271	1.00[AMR][1000 genomes]
rs72699278	1.00[AMR][1000 genomes]
rs72699280	1.00[AMR][1000 genomes]
rs72699294	1.00[AMR][1000 genomes]
rs72699297	1.00[AMR][1000 genomes]
rs72701016	1.00[AMR][1000 genomes]
rs72701019	1.00[AMR][1000 genomes]
rs72701027	1.00[AMR][1000 genomes]
rs72701031	1.00[AMR][1000 genomes]
rs72701032	1.00[AMR][1000 genomes]
rs72701034	1.00[AMR][1000 genomes]
rs72701040	1.00[AMR][1000 genomes]
rs72701043	1.00[AMR][1000 genomes]
rs72701071	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525665	chr14:84596803-84598224	Enhancers	n/a	n/a	inside rSNPs	n/a
2	nsv528960	chr14:84596803-84598224	Enhancers	n/a	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	chr14:84596800-84597000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

Quick Search:

Input of quick search could be:

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

what's new

Quick links