Variant report

Variant	rs72911368
Chromosome Location	chr4:118818644-118818645
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10004800	1.00[EUR][1000 genomes]
rs10034646	1.00[EUR][1000 genomes]
rs12651118	1.00[AMR][1000 genomes]
rs59783133	1.00[AMR][1000 genomes]
rs72903395	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72905214	1.00[EUR][1000 genomes]
rs72911370	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72913437	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72913439	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72913442	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72913445	1.00[AMR][1000 genomes]
rs72913447	1.00[EUR][1000 genomes]
rs72913461	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72915443	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7699041	1.00[AMR][1000 genomes];1.00[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	nsv482390	chr4:118804378-118944823	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	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	chr4:118813800-118821600	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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